A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149703



Internal ID15853292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36663856..36698329hg38UCSC Ensembl
Innerchr17:35020291..35054772hg19UCSC Ensembl
Innerchr17:32094404..32128885hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3834474
hg1934482
hg1834482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574916
Supporting Variants
Samples1780854065_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149703
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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