A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575921



Internal ID16016644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67993532..67994276hg38UCSC Ensembl
Innerchr17:65989648..65990392hg19UCSC Ensembl
Innerchr17:63420110..63420854hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38745
hg19745
hg18745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5755n54
Supporting Variantsnssv875902
Samples
Known GenesC17orf58
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575921
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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