A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3524649



Internal ID18822930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:80025926..80051324hg38UCSC Ensembl
Innerchr12:80419706..80445104hg19UCSC Ensembl
Innerchr12:78943837..78969235hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3825399
hg1925399
hg1825399
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050277
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)nssv3524649
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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