A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35059



Internal ID12991095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57133333..57177149hg38UCSC Ensembl
Innerchr10:58893093..58936909hg19UCSC Ensembl
Innerchr10:58563099..58606915hg18UCSC Ensembl
Innerchr10:58563099..58606915hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3843817
hg1943817
hg1843817
hg1743817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv31e55
Supporting Variantsessv6978270, essv6987361
SamplesNA18995
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35059
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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