A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979562



Internal ID12980390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57812923..58011708hg38UCSC Ensembl
Innerchr10:59572683..59771468hg19UCSC Ensembl
Innerchr10:59242689..59441474hg18UCSC Ensembl
Innerchr10:59242689..59441474hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38198786
hg19198786
hg18198786
hg17198786
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)essv6979562
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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