A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv960911



Internal ID15908181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28428339..28685723hg38UCSC Ensembl
Innerchr3:28469830..28727214hg19UCSC Ensembl
Innerchr3:28444834..28702218hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38257385
hg19257385
hg18257385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590010
Supporting Variants
Samples
Known GenesLINC00693, ZCWPW2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv960911
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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