A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573882



Internal ID16014605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:170860..181222hg38UCSC Ensembl
Innerchr17:20651..31013hg19UCSC Ensembl
Innerchr17:20651..31013hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3810363
hg1910363
hg1810363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5347n54
Supporting Variantsnssv864154, nssv864153, nssv864152, nssv864151
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573882
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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