A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv870168



Internal ID16164124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:37387113..37398642hg38UCSC Ensembl
Innerchr17:35744048..35758648hg19UCSC Ensembl
Innerchr17:32818161..32832761hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3811530
hg1914601
hg1814601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574928
Supporting Variants
Samples
Known GenesACACA, C17orf78
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv870168
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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