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nsv6140866

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 63 SVs from 23 studies. See in: genome view    
Submitted genomic181,353,000-181,368,000Question Mark
Overlapping variant regions from other studies: 63 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):180,780,001-180,795,001Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6140866Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr5181,353,000181,368,000
nsv6140866RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr5180,780,001180,795,001

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16977911duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16977911Submitted genomicNC_000005.10:g.181
353000_181368000du
p
GRCh38 (hg38)NC_000005.10Chr5181,353,000181,368,000
nssv16977911RemappedPerfectNC_000005.9:g.1807
80001_180795001dup
GRCh37.p13First PassNC_000005.9Chr5180,780,001180,795,001

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)
nssv169779110.004143748
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