A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575939



Internal ID16363348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70205218..70217684hg38UCSC Ensembl
Innerchr17:68201359..68213825hg19UCSC Ensembl
Innerchr17:65712954..65725420hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3812467
hg1912467
hg1812467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875918, nssv875919
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575939
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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