A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv870540



Internal ID15817810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:40910399..40979621hg38UCSC Ensembl
Innerchr17:39066651..39135873hg19UCSC Ensembl
Innerchr17:36320177..36389399hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3869223
hg1969223
hg1869223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574999
Supporting Variants
Samples
Known GenesKRT23, KRT39, KRT40
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv870540
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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