A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980095



Internal ID12981250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1810597..1875160hg38UCSC Ensembl
Innerchr10:1852791..1917354hg19UCSC Ensembl
Innerchr10:1842791..1907354hg18UCSC Ensembl
Innerchr10:1842791..1907354hg17UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3864564
hg1964564
hg1864564
hg1764564
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34804
Supporting Variants
SamplesNA18952
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980095
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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