A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958862



Internal ID16252818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8779046..8816277hg38UCSC Ensembl
Innerchr3:8820732..8857963hg19UCSC Ensembl
Innerchr3:8795732..8832963hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3837232
hg1937232
hg1837232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589621
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)nssv958862
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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