A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039320



Internal ID18781851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52294888..52378919hg38UCSC Ensembl
Innerchr12:52688672..52772703hg19UCSC Ensembl
Innerchr12:50974939..51058970hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg3884032
hg1984032
hg1884032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1503n100
Supporting Variantsnssv3523555
Samples
Known GenesKRT83, KRT84, KRT85, KRT86
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039320
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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