A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599379



Internal ID18897660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11828011..11873965hg38UCSC Ensembl
Innerchr20:11808659..11854613hg19UCSC Ensembl
Innerchr20:11756659..11802613hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3845955
hg1945955
hg1845955
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058532
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3599379
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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