nsv5563185

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,471

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 27 studies. See in: genome view    
Submitted genomic46,388,537-46,391,007Question Mark
Overlapping variant regions from other studies: 92 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):46,410,087-46,412,557Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563185Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1146,388,53746,391,007
nsv5563185RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1146,410,08746,412,557

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17047336sequence alterationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStop
nssv17047336Submitted genomicGRCh38 (hg38)NC_000011.10Chr1146,388,53746,391,007
nssv17047336RemappedPerfectGRCh37.p13First PassNC_000011.9Chr1146,410,08746,412,557

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)
nssv17047336<0.00126404
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