A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978769



Internal ID12632407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:52282619..52383252hg38UCSC Ensembl
Innerchr12:52676403..52777036hg19UCSC Ensembl
Innerchr12:50962670..51063303hg18UCSC Ensembl
Innerchr12:50962670..51063303hg17UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38100634
hg19100634
hg18100634
hg17100634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35152
Supporting Variants
SamplesNA12239
Known GenesKRT81, KRT83, KRT84, KRT85, KRT86
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978769
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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