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nsv5916843

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:28,719

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 295 SVs from 45 studies. See in: genome view    
Submitted genomic134,026,732-134,055,450Question Mark
Overlapping variant regions from other studies: 295 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):136,891,854-136,920,572Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5916843Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr9134,026,732134,055,450
nsv5916843RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9136,891,854136,920,572

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17432134duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17432134Submitted genomicNC_000009.12:g.134
026732_134055450du
p
GRCh38 (hg38)NC_000009.12Chr9134,026,732134,055,450
nssv17432134RemappedPerfectNC_000009.11:g.136
891854_136920572du
p
GRCh37.p13First PassNC_000009.11Chr9136,891,854136,920,572

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)
nssv174321340.00111820
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