U.S. flag

An official website of the United States government

nsv1158568

  • 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: 77 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):53,865,585-53,865,585Question Mark
Overlapping variant regions from other studies: 263 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):19,054,415-19,054,415Question Mark
Overlapping variant regions from other studies: 77 SVs from 20 studies. See in: genome view    
Submitted genomic53,933,278-53,933,278Question Mark
Overlapping variant regions from other studies: 269 SVs from 29 studies. See in: genome view    
Submitted genomic19,054,413-19,054,413Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv1158568RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr753,865,58553,865,585-
nsv1158568RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr919,054,41519,054,415-
nsv1158568Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr753,933,27853,933,278-
nsv1158568Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr919,054,41319,054,413-

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv4025986interchromosomal translocationKWS1SequencingRead depth and paired-end mapping22,470

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv4025986RemappedPerfectGRCh38.p12First PassNC_000007.14Chr753,865,58553,865,585-
nssv4025986RemappedPerfectGRCh38.p12First PassNC_000009.12Chr919,054,41519,054,415-
nssv4025986Submitted genomicGRCh37 (hg19)NC_000007.13Chr753,933,27853,933,278-
nssv4025986Submitted genomicGRCh37 (hg19)NC_000009.11Chr919,054,41319,054,413-

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