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nsv5470931

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,129

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 255 SVs from 27 studies. See in: genome view    
Submitted genomic2,305,974-2,307,102Question Mark
Overlapping variant regions from other studies: 255 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):2,306,088-2,307,216Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5470931Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr52,305,9742,307,102
nsv5470931RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr52,306,0882,307,216

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16963453deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16963453Submitted genomicNC_000005.10:g.230
5974_2307102del
GRCh38 (hg38)NC_000005.10Chr52,305,9742,307,102
nssv16963453RemappedPerfectNC_000005.9:g.2306
088_2307216del
GRCh37.p13First PassNC_000005.9Chr52,306,0882,307,216

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)
nssv16963453<0.00136404
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