A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979631



Internal ID12633838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:19520745..19698715hg38UCSC Ensembl
Innerchr10:19809674..19987644hg19UCSC Ensembl
Innerchr10:19849680..20027650hg18UCSC Ensembl
Innerchr10:19849680..20027650hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38177971
hg19177971
hg18177971
hg17177971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34306
Supporting Variants
SamplesNA18592
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979631
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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