A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2750851



Internal ID12984403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108744030..109145453hg38UCSC Ensembl
Innerchr10:110503788..110905211hg19UCSC Ensembl
Innerchr10:110493778..110895201hg18UCSC Ensembl
Innerchr10:110493778..110895201hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38401424
hg19401424
hg18401424
hg17401424
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6986447, essv6983473, essv6983475, essv6986448, essv6983474
SamplesBEC_660
Known Genes
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)esv2750851
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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