A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983197



Internal ID12628283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:64321324..64492209hg38UCSC Ensembl
Innerchr10:66081084..66251966hg19UCSC Ensembl
Innerchr10:65751090..65921972hg18UCSC Ensembl
Innerchr10:65751090..65921972hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38170886
hg19170883
hg18170883
hg17170883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2750967
Supporting Variants
SamplesBEC_554
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983197
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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