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nsv5429547

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:695,308

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1889 SVs from 86 studies. See in: genome view    
Submitted genomic27,306,072-28,001,379Question Mark
Overlapping variant regions from other studies: 1897 SVs from 86 studies. See in: genome view    
Remapped(Score: Good):27,632,563-28,327,890Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5429547Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr127,306,07228,001,379
nsv5429547RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr127,632,56328,327,890

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16900441deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16900441Submitted genomicNC_000001.11:g.273
06072_28001379del
GRCh38 (hg38)NC_000001.11Chr127,306,07228,001,379
nssv16900441RemappedGoodNC_000001.10:g.276
32563_28327890del
GRCh37.p13First PassNC_000001.10Chr127,632,56328,327,890

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)
nssv16900441<0.00116404
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