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nsv5442025

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,246

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 171 SVs from 36 studies. See in: genome view    
Submitted genomic46,925,512-46,931,757Question Mark
Overlapping variant regions from other studies: 171 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):47,152,651-47,158,896Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5442025Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr246,925,51246,931,757
nsv5442025RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr247,152,65147,158,896

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16913274deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16913274Submitted genomicNC_000002.12:g.469
25512_46931757del
GRCh38 (hg38)NC_000002.12Chr246,925,51246,931,757
nssv16913274RemappedPerfectNC_000002.11:g.471
52651_47158896del
GRCh37.p13First PassNC_000002.11Chr247,152,65147,158,896

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)
nssv169132740.00186404
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