A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875917



Internal ID16169873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69659978..69833317hg38UCSC Ensembl
Innerchr17:67656119..67829458hg19UCSC Ensembl
Innerchr17:65167714..65341053hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38173340
hg19173340
hg18173340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575938
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)nssv875917
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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