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nsv6179712

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:80

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 140 SVs from 28 studies. See in: genome view    
Submitted genomic44,181,494-44,181,573Question Mark
Overlapping variant regions from other studies: 140 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):44,149,231-44,149,310Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6179712Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr644,181,49444,181,573
nsv6179712RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr644,149,23144,149,310

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17880624deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17880624Submitted genomicNC_000006.12:g.441
81494_44181573del
GRCh38 (hg38)NC_000006.12Chr644,181,49444,181,573
nssv17880624RemappedPerfectNC_000006.11:g.441
49231_44149310del
GRCh37.p13First PassNC_000006.11Chr644,149,23144,149,310

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)
nssv17880624<0.00122110
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