A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573880



Internal ID16014603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:170860..181019hg38UCSC Ensembl
Innerchr17:20651..30810hg19UCSC Ensembl
Innerchr17:20651..30810hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3810160
hg1910160
hg1810160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5347n54
Supporting Variantsnssv864148, nssv864147, nssv864146, nssv864149
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573880
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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