A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv870535



Internal ID15817805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40563547..40668384hg38UCSC Ensembl
Innerchr17:38719799..38824636hg19UCSC Ensembl
Innerchr17:35973325..36078162hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38104838
hg19104838
hg18104838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574994
Supporting Variants
Samples
Known GenesCCR7, KRT222, SMARCE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv870535
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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