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nsv5449506

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:846

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 186 SVs from 27 studies. See in: genome view    
Submitted genomic49,150,068-49,150,913Question Mark
Overlapping variant regions from other studies: 186 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):49,377,207-49,378,052Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449506Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr249,150,06849,150,913
nsv5449506RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr249,377,20749,378,052

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16912705deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16912705Submitted genomicNC_000002.12:g.491
50068_49150913del
GRCh38 (hg38)NC_000002.12Chr249,150,06849,150,913
nssv16912705RemappedPerfectNC_000002.11:g.493
77207_49378052del
GRCh37.p13First PassNC_000002.11Chr249,377,20749,378,052

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)
nssv16912705<0.00146404
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