A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575456



Internal ID16362865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46771382..46772165hg38UCSC Ensembl
Innerchr17:44848748..44849531hg19UCSC Ensembl
Innerchr17:42203916..42204694hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38784
hg19784
hg18779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5673n54
Supporting Variantsnssv873057
Samples
Known GenesWNT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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