A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986447



Internal ID12976361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108924243..109117486hg38UCSC Ensembl
Innerchr10:110684001..110877244hg19UCSC Ensembl
Innerchr10:110673991..110867234hg18UCSC Ensembl
Innerchr10:110673991..110867234hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38193244
hg19193244
hg18193244
hg17193244
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6986447
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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