A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986781



Internal ID12632884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75795733..75912395hg38UCSC Ensembl
Innerchr10:77555491..77672153hg19UCSC Ensembl
Innerchr10:77225497..77342159hg18UCSC Ensembl
Innerchr10:77225497..77342159hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38116663
hg19116663
hg18116663
hg17116663
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34687
Supporting Variants
SamplesNA12872
Known GenesC10orf11
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986781
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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