A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979563



Internal ID12980389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57812934..58011734hg38UCSC Ensembl
Innerchr10:59572694..59771494hg19UCSC Ensembl
Innerchr10:59242700..59441500hg18UCSC Ensembl
Innerchr10:59242700..59441500hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38198801
hg19198801
hg18198801
hg17198801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35063
Supporting Variants
SamplesNA18572
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979563
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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