A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv874076



Internal ID16168032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:55375742..55390852hg38UCSC Ensembl
Innerchr17:53453103..53468213hg19UCSC Ensembl
Innerchr17:50808102..50823212hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3815111
hg1915111
hg1815111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575665
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)nssv874076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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