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nsv4131692

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:171,041

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 15 studies. See in: genome view    
Remapped(Score: Good):134,433,832-134,604,872Question Mark
Overlapping variant regions from other studies: 119 SVs from 15 studies. See in: genome view    
Submitted genomic133,769,523-133,940,562Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4131692RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr5134,433,832134,604,872
nsv4131692Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr5133,769,523133,940,562

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15903456deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15903456RemappedGoodNC_000005.10:g.134
433832_134604872de
l
GRCh38.p12First PassNC_000005.10Chr5134,433,832134,604,872
nssv15903456Submitted genomicNC_000005.9:g.1337
69523_133940562del
GRCh37.p13NC_000005.9Chr5133,769,523133,940,562

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv159034564.6e-005121694
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