U.S. flag

An official website of the United States government

nsv482405

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:150,618

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 513 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):238,020,395-238,171,012Question Mark
Overlapping variant regions from other studies: 518 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):238,183,695-238,334,312Question Mark
Overlapping variant regions from other studies: 1 SVs from 1 studies. See in: genome view    
Submitted genomic235,224,844-235,375,461Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv482405RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1238,020,395238,171,012
nsv482405RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1238,183,695238,334,312
nsv482405Submitted genomicNCBI34 (hg16)Primary AssemblyNC_000001.7Chr1235,224,844235,375,461

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv3009614copy number lossBAC aCGHProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv3009614RemappedPerfectNC_000001.11:g.(?_
238020395)_(238171
012_?)del
GRCh38.p12First PassNC_000001.11Chr1238,020,395238,171,012
nssv3009614RemappedPerfectNC_000001.10:g.(?_
238183695)_(238334
312_?)del
GRCh37.p13First PassNC_000001.10Chr1238,183,695238,334,312
nssv3009614Submitted genomicNC_000001.7:g.(?_2
35224844)_(2353754
61_?)del
NCBI34 (hg16)NC_000001.7Chr1235,224,844235,375,461

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

Support Center