A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989085



Internal ID12633313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20400771..20522542hg38UCSC Ensembl
Innerchr13:20974910..21096681hg19UCSC Ensembl
Innerchr13:19872910..19994681hg18UCSC Ensembl
Innerchr13:19872910..19994681hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38121772
hg19121772
hg18121772
hg17121772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34984
Supporting Variants
SamplesNA18529
Known GenesCRYL1, MIR4499
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989085
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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