A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872983



Internal ID16166939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46771072..46771995hg38UCSC Ensembl
Innerchr17:44848438..44849361hg19UCSC Ensembl
Innerchr17:42203606..42204524hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38924
hg19924
hg18919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575437
Supporting Variants
Samples
Known GenesWNT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872983
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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