A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983475



Internal ID12976371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108947193..109084997hg38UCSC Ensembl
Innerchr10:110706951..110844755hg19UCSC Ensembl
Innerchr10:110696941..110834745hg18UCSC Ensembl
Innerchr10:110696941..110834745hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38137805
hg19137805
hg18137805
hg17137805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750851
Supporting Variants
SamplesBEC_660
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983475
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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