A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989891



Internal ID12977480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86058462..86166464hg38UCSC Ensembl
Innerchr13:86632597..86740599hg19UCSC Ensembl
Innerchr13:85530598..85638600hg18UCSC Ensembl
Innerchr13:85530598..85638600hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38108003
hg19108003
hg18108003
hg17108003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751155
Supporting Variants
SamplesBEC_74
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989891
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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