A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34583



Internal ID12990620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57123412..57177149hg38UCSC Ensembl
Innerchr10:58883172..58936909hg19UCSC Ensembl
Innerchr10:58553178..58606915hg18UCSC Ensembl
Innerchr10:58553178..58606915hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3853738
hg1953738
hg1853738
hg1753738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv31e55
Supporting Variantsessv6989102, essv6988198
SamplesNA18572
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)esv34583
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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