A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989904



Internal ID12977597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60087434..60130333hg38UCSC Ensembl
Innerchr3:60073160..60116060hg19UCSC Ensembl
Innerchr3:60048200..60091100hg18UCSC Ensembl
Innerchr3:60048200..60091100hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3842900
hg1942901
hg1842901
hg1742901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752011
Supporting Variants
SamplesBEC_759
Known GenesFHIT
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989904
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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