A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574999



Internal ID16015722
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 StatusM
Merged Variants
Supporting Variantsnssv870540
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)nsv574999
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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