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nsv5461617

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,849

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 102 SVs from 23 studies. See in: genome view    
Submitted genomic35,464,426-35,467,274Question Mark
Overlapping variant regions from other studies: 102 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):35,432,203-35,435,051Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5461617Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr635,464,42635,467,274
nsv5461617RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr635,432,20335,435,051

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16983599deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16983599Submitted genomicNC_000006.12:g.354
64426_35467274del
GRCh38 (hg38)NC_000006.12Chr635,464,42635,467,274
nssv16983599RemappedPerfectNC_000006.11:g.354
32203_35435051del
GRCh37.p13First PassNC_000006.11Chr635,432,20335,435,051

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)
nssv16983599<0.00116404
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