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nsv886702

  • Variant Calls:12
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:142,538

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 765 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):140,581,682-140,724,219Question Mark
Overlapping variant regions from other studies: 765 SVs from 70 studies. See in: genome view    
Remapped(Score: Perfect):140,902,819-141,045,356Question Mark
Overlapping variant regions from other studies: 180 SVs from 17 studies. See in: genome view    
Submitted genomic140,944,512-141,087,049Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv886702RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nsv886702RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nsv886702Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1532043copy number lossMS10699SNP arraySNP genotyping analysis39
nssv1537933copy number lossMS13426SNP arraySNP genotyping analysis38
nssv1566032copy number lossIS30562SNP arraySNP genotyping analysis16
nssv1566753copy number lossIS30899SNP arraySNP genotyping analysis39
nssv1567010copy number lossIS31041SNP arraySNP genotyping analysis83
nssv1569266copy number lossIS31554SNP arraySNP genotyping analysis56
nssv1569642copy number lossIS31652SNP arraySNP genotyping analysis16
nssv1570455copy number lossIS32015SNP arraySNP genotyping analysis16
nssv1582801copy number lossIS36170SNP arraySNP genotyping analysis26
nssv1582961copy number lossIS36219SNP arraySNP genotyping analysis125
nssv1583528copy number lossIS36527SNP arraySNP genotyping analysis45
nssv1591928copy number lossIS39100SNP arraySNP genotyping analysis20

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1532043RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1537933RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1566032RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1566753RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1567010RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1569266RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1569642RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1570455RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1582801RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1582961RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1583528RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1591928RemappedPerfectNC_000006.12:g.(14
0581682_140590252)
_(140720192_140724
219)del
GRCh38.p12First PassNC_000006.12Chr6140,581,682140,590,252140,720,192140,724,219
nssv1532043RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1537933RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1566032RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1566753RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1567010RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1569266RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1569642RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1570455RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1582801RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1582961RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1583528RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1591928RemappedPerfectNC_000006.11:g.(14
0902819_140911389)
_(141041329_141045
356)del
GRCh37.p13First PassNC_000006.11Chr6140,902,819140,911,389141,041,329141,045,356
nssv1532043Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1537933Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1566032Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1566753Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1567010Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1569266Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1569642Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1570455Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1582801Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1582961Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1583528Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049
nssv1591928Submitted genomicNC_000006.10:g.(14
0944512_140953082)
_(141083022_141087
049)del
NCBI36 (hg18)NC_000006.10Chr6140,944,512140,953,082141,083,022141,087,049

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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