A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34687



Internal ID12644037
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 StatusM
Merged Variants
Supporting Variantsessv6986782, essv6979047, essv6979049, essv6979048, essv6986781
SamplesNA12872
Known GenesC10orf11
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34687
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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