A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988189



Internal ID12980295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:57133333..57188447hg38UCSC Ensembl
Innerchr10:58893093..58948207hg19UCSC Ensembl
Innerchr10:58563099..58618213hg18UCSC Ensembl
Innerchr10:58563099..58618213hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3855115
hg1955115
hg1855115
hg1755115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34551
Supporting Variants
SamplesNA18564
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988189
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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