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nsv4191916

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:51

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 88 SVs from 9 studies. See in: genome view    
Remapped(Score: Perfect):137,243,960-137,244,010Question Mark
Overlapping variant regions from other studies: 88 SVs from 9 studies. See in: genome view    
Submitted genomic140,138,412-140,138,462Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4191916RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9137,243,960137,244,010
nsv4191916Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr9140,138,412140,138,462

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15939164deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15939164RemappedPerfectNC_000009.12:g.137
243960_137244010de
l
GRCh38.p12First PassNC_000009.12Chr9137,243,960137,244,010
nssv15939164Submitted genomicNC_000009.11:g.140
138412_140138462de
l
GRCh37.p13NC_000009.11Chr9140,138,412140,138,462

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)
nssv159391644.6e-005121694
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