A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868962



Internal ID16162918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:22605783..22743028hg38UCSC Ensembl
Innerchr17:22105110..22242355hg19UCSC Ensembl
Innerchr17:22029237..22166482hg18UCSC Ensembl
Cytoband17p11.1
Allele length
AssemblyAllele length
hg38137246
hg19137246
hg18137246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574624
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868962
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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