A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083687



Internal ID21290267
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 StatusS
Merged Variantsnsv3117929
Supporting Variants
Samplessample58
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083687
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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