A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34957



Internal ID12990993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98262439..98289945hg38UCSC Ensembl
Innerchr13:98914693..98942199hg19UCSC Ensembl
Innerchr13:97712694..97740200hg18UCSC Ensembl
Innerchr13:97712694..97740200hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3827507
hg1927507
hg1827507
hg1727507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6988258, essv6979861
SamplesNA18854
Known GenesFARP1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34957
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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