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nsv906206

  • Variant Calls:12
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:72,749

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2474 SVs from 91 studies. See in: genome view    
Remapped(Score: Perfect):32,520,341-32,593,089Question Mark
Overlapping variant regions from other studies: 2474 SVs from 91 studies. See in: genome view    
Remapped(Score: Perfect):32,531,662-32,604,410Question Mark
Overlapping variant regions from other studies: 1563 SVs from 30 studies. See in: genome view    
Submitted genomic32,439,163-32,511,911Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv906206RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nsv906206RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nsv906206Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1505167copy number lossSP53287SNP arraySNP genotyping analysis14
nssv1521120copy number lossSP52220SNP arraySNP genotyping analysis5
nssv1523614copy number lossSP54117SNP arraySNP genotyping analysis11
nssv1523959copy number lossSP54311SNP arraySNP genotyping analysis8
nssv1525142copy number lossSP55531SNP arraySNP genotyping analysis8
nssv1532929copy number lossMS10946SNP arraySNP genotyping analysis13
nssv1535180copy number lossMS12055SNP arraySNP genotyping analysis10
nssv1540483copy number lossMS14855SNP arraySNP genotyping analysis14
nssv1548056copy number lossMS17689SNP arraySNP genotyping analysis17
nssv1548401copy number lossMS17825SNP arraySNP genotyping analysis32
nssv1552220copy number lossMS19292SNP arraySNP genotyping analysis6
nssv1557233copy number lossMS22505SNP arraySNP genotyping analysis14

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1505167RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1521120RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1523614RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1523959RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1525142RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1532929RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1535180RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1540483RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1548056RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1548401RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1552220RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1557233RemappedPerfectNC_000016.10:g.(32
520341_32520438)_(
32586373_32593089)
del
GRCh38.p12First PassNC_000016.10Chr1632,520,34132,520,43832,586,37332,593,089
nssv1505167RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1521120RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1523614RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1523959RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1525142RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1532929RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1535180RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1540483RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1548056RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1548401RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1552220RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1557233RemappedPerfectNC_000016.9:g.(325
31662_32531759)_(3
2597694_32604410)d
el
GRCh37.p13First PassNC_000016.9Chr1632,531,66232,531,75932,597,69432,604,410
nssv1505167Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1521120Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1523614Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1523959Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1525142Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1532929Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1535180Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1540483Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1548056Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1548401Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1552220Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911
nssv1557233Submitted genomicNC_000016.8:g.(324
39163_32439260)_(3
2505195_32511911)d
el
NCBI36 (hg18)NC_000016.8Chr1632,439,16332,439,26032,505,19532,511,911

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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