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nsv5432514

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:247

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 206 SVs from 34 studies. See in: genome view    
Submitted genomic74,197,460-74,197,706Question Mark
Overlapping variant regions from other studies: 206 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):74,663,144-74,663,390Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5432514Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr174,197,46074,197,706
nsv5432514RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr174,663,14474,663,390

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16904643deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16904643Submitted genomicNC_000001.11:g.741
97460_74197706del
GRCh38 (hg38)NC_000001.11Chr174,197,46074,197,706
nssv16904643RemappedPerfectNC_000001.10:g.746
63144_74663390del
GRCh37.p13First PassNC_000001.10Chr174,663,14474,663,390

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)
nssv16904643<0.00136404
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