A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979047



Internal ID12632867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:75795733..75976864hg38UCSC Ensembl
Innerchr10:77555491..77736622hg19UCSC Ensembl
Innerchr10:77225497..77406628hg18UCSC Ensembl
Innerchr10:77225497..77406628hg17UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38181132
hg19181132
hg18181132
hg17181132
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)essv6979047
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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