A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982333



Internal ID12973589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80716859..80808928hg38UCSC Ensembl
Innerchr10:82476615..82568684hg19UCSC Ensembl
Innerchr10:82466595..82558664hg18UCSC Ensembl
Innerchr10:82466595..82558664hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3892070
hg1992070
hg1892070
hg1792070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750975
Supporting Variants
SamplesBEC_424
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982333
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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