A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34654



Internal ID12990690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105845347..105922618hg38UCSC Ensembl
Innerchr10:107605105..107682376hg19UCSC Ensembl
Innerchr10:107595095..107672366hg18UCSC Ensembl
Innerchr10:107595095..107672366hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3877272
hg1977272
hg1877272
hg1777272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv34e55
Supporting Variantsessv6980248, essv6987745
SamplesNA06991
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)esv34654
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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