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nsv4518016

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 27 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):160,234,598-160,234,652Question Mark
Overlapping variant regions from other studies: 27 SVs from 6 studies. See in: genome view    
Submitted genomic160,204,388-160,204,442Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4518016RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1160,234,598160,234,652
nsv4518016Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr1160,204,388160,204,442

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15962763duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15962763RemappedPerfectNC_000001.11:g.160
234598_160234652du
p
GRCh38.p12First PassNC_000001.11Chr1160,234,598160,234,652
nssv15962763Submitted genomicNC_000001.10:g.160
204388_160204442du
p
GRCh37.p13NC_000001.10Chr1160,204,388160,204,442

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)
nssv15962763<0.001321694
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