A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988521



Internal ID12973588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80713264..80805764hg38UCSC Ensembl
Innerchr10:82473020..82565520hg19UCSC Ensembl
Innerchr10:82463000..82555500hg18UCSC Ensembl
Innerchr10:82463000..82555500hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3892501
hg1992501
hg1892501
hg1792501
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988521
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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