A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868981



Internal ID16162937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:27155725..27164439hg38UCSC Ensembl
Innerchr17:25482751..25491465hg19UCSC Ensembl
Innerchr17:22506878..22515592hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg388715
hg198715
hg188715
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574639
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868981
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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