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nsv4218878

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,112,839

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1989 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):50,257,603-53,370,441Question Mark
Overlapping variant regions from other studies: 1989 SVs from 21 studies. See in: genome view    
Submitted genomic50,724,321-53,837,159Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4218878RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000014.9Chr1450,257,60353,370,441
nsv4218878Submitted genomicGRCh37.p13Primary AssemblyNC_000014.8Chr1450,724,32153,837,159

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15952721duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15952721RemappedPerfectNC_000014.9:g.5025
7603_53370441dup
GRCh38.p12First PassNC_000014.9Chr1450,257,60353,370,441
nssv15952721Submitted genomicNC_000014.8:g.5072
4321_53837159dup
GRCh37.p13NC_000014.8Chr1450,724,32153,837,159

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)
nssv159527214.6e-005121694
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