A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979805



Internal ID12634094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:77610736..77746636hg38UCSC Ensembl
Innerchr10:79370494..79506394hg19UCSC Ensembl
Innerchr10:79040500..79176400hg18UCSC Ensembl
Innerchr10:79040500..79176400hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38135901
hg19135901
hg18135901
hg17135901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34251
Supporting Variants
SamplesNA18633
Known GenesKCNMA1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979805
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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