A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151812



Internal ID15876565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153019529..153120250hg38UCSC Ensembl
Innerchr3:152737318..152838039hg19UCSC Ensembl
Innerchr3:154220008..154320729hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38100722
hg19100722
hg18100722
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592074
Supporting Variants
SamplesHGDP00862
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151812
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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