A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575193



Internal ID16015916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46172742..46190497hg38UCSC Ensembl
Innerchr17:44250108..44267863hg19UCSC Ensembl
Innerchr17:41605885..41623640hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3817756
hg1917756
hg1817756
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5625n54
Supporting Variantsnssv872432
Samples
Known GenesKANSL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575193
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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