A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983585



Internal ID12629854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98099931..98147329hg38UCSC Ensembl
Innerchr13:98752185..98799583hg19UCSC Ensembl
Innerchr13:97550186..97597584hg18UCSC Ensembl
Innerchr13:97550186..97597584hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3847399
hg1947399
hg1847399
hg1747399
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751157
Supporting Variants
SamplesBEC_670
Known GenesFARP1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983585
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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