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nsv872711

  • Variant Calls:17
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:91,336

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 715 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):189,559,813-189,651,148Question Mark
Overlapping variant regions from other studies: 715 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):189,528,943-189,620,278Question Mark
Overlapping variant regions from other studies: 227 SVs from 23 studies. See in: genome view    
Submitted genomic187,795,566-187,886,901Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv872711RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nsv872711RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nsv872711Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1552966copy number lossMS19677SNP arraySNP genotyping analysis15
nssv1572059copy number lossIS32850SNP arraySNP genotyping analysis9
nssv1574106copy number lossIS33514SNP arraySNP genotyping analysis56
nssv1576483copy number lossIS34066SNP arraySNP genotyping analysis13
nssv1576850copy number lossIS34271SNP arraySNP genotyping analysis11
nssv1577816copy number lossIS34573SNP arraySNP genotyping analysis23
nssv1578439copy number lossIS34779SNP arraySNP genotyping analysis22
nssv1583833copy number lossIS36678SNP arraySNP genotyping analysis9
nssv1585672copy number lossIS37612SNP arraySNP genotyping analysis9
nssv1586784copy number lossIS37979SNP arraySNP genotyping analysis10
nssv1587200copy number lossIS37995SNP arraySNP genotyping analysis15
nssv1588758copy number lossIS38241SNP arraySNP genotyping analysis16
nssv1589656copy number lossIS38394SNP arraySNP genotyping analysis9
nssv1590040copy number lossIS38448SNP arraySNP genotyping analysis8
nssv1593055copy number lossIS39348SNP arraySNP genotyping analysis10
nssv1594679copy number lossIS39996SNP arraySNP genotyping analysis14
nssv1600494copy number lossIS41892SNP arraySNP genotyping analysis12

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1552966RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1572059RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1574106RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1576483RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1576850RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1577816RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1578439RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1583833RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1585672RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1586784RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1587200RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1588758RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1589656RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1590040RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1593055RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1594679RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1600494RemappedPerfectNC_000001.11:g.(18
9559813_189567152)
_(189639542_189651
148)del
GRCh38.p12First PassNC_000001.11Chr1189,559,813189,567,152189,639,542189,651,148
nssv1552966RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1572059RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1574106RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1576483RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1576850RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1577816RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1578439RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1583833RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1585672RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1586784RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1587200RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1588758RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1589656RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1590040RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1593055RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1594679RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1600494RemappedPerfectNC_000001.10:g.(18
9528943_189536282)
_(189608672_189620
278)del
GRCh37.p13First PassNC_000001.10Chr1189,528,943189,536,282189,608,672189,620,278
nssv1552966Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1572059Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1574106Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1576483Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1576850Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1577816Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1578439Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1583833Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1585672Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1586784Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1587200Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1588758Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1589656Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1590040Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1593055Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1594679Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901
nssv1600494Submitted genomicNC_000001.9:g.(187
795566_187802905)_
(187875295_1878869
01)del
NCBI36 (hg18)NC_000001.9Chr1187,795,566187,802,905187,875,295187,886,901

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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