A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976855



Internal ID15924125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155761433..155794055hg38UCSC Ensembl
Innerchr3:155479222..155511844hg19UCSC Ensembl
Innerchr3:156961916..156994538hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3832623
hg1932623
hg1832623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592080
Supporting Variants
Samples
Known GenesC3orf33
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976855
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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