A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575952



Internal ID16363361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71330442..71374954hg38UCSC Ensembl
Innerchr17:69326583..69371095hg19UCSC Ensembl
Innerchr17:66838178..66882690hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3844513
hg1944513
hg1844513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149799
Samples1798860114_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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