A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv960912



Internal ID16254868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28739222..29002946hg38UCSC Ensembl
Innerchr3:28780713..29044437hg19UCSC Ensembl
Innerchr3:28755717..29019441hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38263725
hg19263725
hg18263725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590011
Supporting Variants
Samples
Known GenesLINC00693
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv960912
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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