A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980074



Internal ID12634530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:91115235..91206548hg38UCSC Ensembl
Innerchr8:92127463..92218776hg19UCSC Ensembl
Innerchr8:92196639..92287952hg18UCSC Ensembl
Innerchr8:92196639..92287952hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3891314
hg1991314
hg1891314
hg1791314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35058
Supporting Variants
SamplesNA18948
Known GenesLRRC69, MIR4661
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980074
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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