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nsv4528489

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:428,383

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 479 SVs from 22 studies. See in: genome view    
Remapped(Score: Pass):49,918,447-50,346,829Question Mark
Overlapping variant regions from other studies: 431 SVs from 22 studies. See in: genome view    
Submitted genomic49,939,999-50,306,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4528489RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1149,918,44750,346,829
nsv4528489Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1149,939,99950,306,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15801192deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15801192RemappedPassNC_000011.10:g.499
18447_50346829del
GRCh38.p12First PassNC_000011.10Chr1149,918,44750,346,829
nssv15801192Submitted genomicNC_000011.9:g.4993
9999_50306000del
GRCh37.p13NC_000011.9Chr1149,939,99950,306,000

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)
nssv158011924.6e-005121694
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