U.S. flag

An official website of the United States government

nsv1159636

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 399 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):63,881,595-63,881,595Question Mark
Overlapping variant regions from other studies: 218 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):30,356,731-30,356,731Question Mark
Overlapping variant regions from other studies: 268 SVs from 51 studies. See in: genome view    
Submitted genomic68,477,329-68,477,329Question Mark
Overlapping variant regions from other studies: 190 SVs from 36 studies. See in: genome view    
Submitted genomic29,591,407-29,591,407Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv1159636RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr963,881,59563,881,595+
nsv1159636RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2030,356,73130,356,731+
nsv1159636Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr968,477,32968,477,329+
nsv1159636Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2029,591,40729,591,407+

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv4024639interchromosomal translocationKWS1SequencingRead depth and paired-end mapping22,470

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv4024639RemappedPerfectGRCh38.p12First PassNC_000009.12Chr963,881,59563,881,595+
nssv4024639RemappedPerfectGRCh38.p12First PassNC_000020.11Chr2030,356,73130,356,731+
nssv4024639Submitted genomicGRCh37 (hg19)NC_000009.11Chr968,477,32968,477,329+
nssv4024639Submitted genomicGRCh37 (hg19)NC_000020.10Chr2029,591,40729,591,407+

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

You are here: NCBI
Support Center