A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574640



Internal ID16362049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27159539..27193610hg38UCSC Ensembl
Innerchr17:25486565..25520636hg19UCSC Ensembl
Innerchr17:22510692..22544763hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3834072
hg1934072
hg1834072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv868982
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574640
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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