A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv864997



Internal ID15812267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:407766..733582hg38UCSC Ensembl
Innerchr17:257557..636822hg19UCSC Ensembl
Innerchr17:257873..583572hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38325817
hg19379266
hg18325700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574059
Supporting Variants
Samples
Known GenesC17orf97, FAM101B, FAM57A, VPS53
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv864997
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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