A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979861



Internal ID12980882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98262445..98289945hg38UCSC Ensembl
Innerchr13:98914699..98942199hg19UCSC Ensembl
Innerchr13:97712700..97740200hg18UCSC Ensembl
Innerchr13:97712700..97740200hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3827501
hg1927501
hg1827501
hg1727501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34957
Supporting Variants
SamplesNA18854
Known GenesFARP1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979861
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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