A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512331



Internal ID18810612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31849350..31908234hg38UCSC Ensembl
Innerchr12:32002284..32061168hg19UCSC Ensembl
Innerchr12:31893551..31952435hg18UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg3858885
hg1958885
hg1858885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049872
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)nssv3512331
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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