A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149684



Internal ID15877735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:5909208..6015242hg38UCSC Ensembl
Innerchr17:5812528..5918562hg19UCSC Ensembl
Innerchr17:5753252..5859286hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38106035
hg19106035
hg18106035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574309
Supporting Variants
SamplesHGDP01036
Known GenesLOC339166
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149684
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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