A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573887



Internal ID16014610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:170860..181795hg38UCSC Ensembl
Innerchr17:20651..31586hg19UCSC Ensembl
Innerchr17:20651..31586hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3810936
hg1910936
hg1810936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5347n54
Supporting Variantsnssv864168, nssv864170, nssv864167, nssv864178, nssv864174, nssv864177, nssv864172, nssv864169, nssv864175, nssv864176, nssv864171, nssv864173
Samples
Known GenesDOC2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573887
Frequency
Sample Size17421
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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