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nsv4178974

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,603

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):137,075,985-137,091,587Question Mark
Overlapping variant regions from other studies: 103 SVs from 10 studies. See in: genome view    
Submitted genomic139,970,437-139,986,039Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4178974RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr9137,075,985137,091,587
nsv4178974Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr9139,970,437139,986,039

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15987360duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15987360RemappedPerfectNC_000009.12:g.137
075985_137091587du
p
GRCh38.p12First PassNC_000009.12Chr9137,075,985137,091,587
nssv15987360Submitted genomicNC_000009.11:g.139
970437_139986039du
p
GRCh37.p13NC_000009.11Chr9139,970,437139,986,039

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)
nssv15987360<0.001321694
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