A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979797



Internal ID12980753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61008243..61067307hg38UCSC Ensembl
Innerchr3:60993915..61052979hg19UCSC Ensembl
Innerchr3:60968955..61028019hg18UCSC Ensembl
Innerchr3:60968955..61028019hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3859065
hg1959065
hg1859065
hg1759065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34680
Supporting Variants
SamplesNA18632
Known GenesFHIT
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979797
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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