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nsv1068360

  • 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: 116 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):84,948,633-84,948,633Question Mark
Overlapping variant regions from other studies: 107 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):84,948,861-84,948,861Question Mark
Overlapping variant regions from other studies: 116 SVs from 30 studies. See in: genome view    
Submitted genomic85,414,977-85,414,977Question Mark
Overlapping variant regions from other studies: 107 SVs from 26 studies. See in: genome view    
Submitted genomic85,415,205-85,415,205Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
nsv1068360RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1484,948,63384,948,633not reported
nsv1068360RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1484,948,86184,948,861not reported
nsv1068360Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr1485,414,97785,414,977not reported
nsv1068360Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000014.8Chr1485,415,20585,415,205not reported

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv3773077intrachromosomal translocationKWP1SequencingRead depth and paired-end mapping11,116

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
nssv3773077RemappedPerfectGRCh38.p12First PassNC_000014.9Chr1484,948,63384,948,633not reported
nssv3773077RemappedPerfectGRCh38.p12First PassNC_000014.9Chr1484,948,86184,948,861not reported
nssv3773077Submitted genomicGRCh37 (hg19)NC_000014.8Chr1485,414,97785,414,977not reported
nssv3773077Submitted genomicGRCh37 (hg19)NC_000014.8Chr1485,415,20585,415,205not reported

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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