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nsv5531056

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:57,119

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 535 SVs from 62 studies. See in: genome view    
Submitted genomic3,601,052-3,658,170Question Mark
Overlapping variant regions from other studies: 535 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):3,504,346-3,561,464Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531056Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr173,601,0523,658,170
nsv5531056RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr173,504,3463,561,464

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17710423deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17710423Submitted genomicNC_000017.11:g.360
1052_3658170del
GRCh38 (hg38)NC_000017.11Chr173,601,0523,658,170
nssv17710423RemappedPerfectNC_000017.10:g.350
4346_3561464del
GRCh37.p13First PassNC_000017.10Chr173,504,3463,561,464

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)
nssv17710423<0.00116400
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