A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117929



Internal ID21301195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170460423..170497553hg38UCSC Ensembl
Innerchr6:170769511..170806641hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3837131
hg1937131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087572, nssv14083687
Samplessample184, sample58
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117929
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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