A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976860



Internal ID16270816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:156109845..156294890hg38UCSC Ensembl
Innerchr3:155827634..156012679hg19UCSC Ensembl
Innerchr3:157310328..157495373hg18UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38185046
hg19185046
hg18185046
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592085
Supporting Variants
Samples
Known GenesKCNAB1, KCNAB1-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976860
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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