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nsv4247886

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:120

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 24 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):28,722,301-28,722,420Question Mark
Overlapping variant regions from other studies: 24 SVs from 6 studies. See in: genome view    
Submitted genomic27,049,319-27,049,438Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4247886RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000017.11Chr1728,722,30128,722,420
nsv4247886Submitted genomicGRCh37.p13Primary AssemblyNC_000017.10Chr1727,049,31927,049,438

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15833747deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15833747RemappedPerfectNC_000017.11:g.287
22301_28722420del
GRCh38.p12First PassNC_000017.11Chr1728,722,30128,722,420
nssv15833747Submitted genomicNC_000017.10:g.270
49319_27049438del
GRCh37.p13NC_000017.10Chr1727,049,31927,049,438

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)
nssv158337474.6e-005121694
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