A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv960103



Internal ID16254059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22491169..22878755hg38UCSC Ensembl
Innerchr3:22532660..22920246hg19UCSC Ensembl
Innerchr3:22507664..22895250hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38387587
hg19387587
hg18387587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589941
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)nssv960103
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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