A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986448



Internal ID12976370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:108947252..109085252hg38UCSC Ensembl
Innerchr10:110707010..110845010hg19UCSC Ensembl
Innerchr10:110697000..110835000hg18UCSC Ensembl
Innerchr10:110697000..110835000hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38138001
hg19138001
hg18138001
hg17138001
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)essv6986448
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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