A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6990092



Internal ID12982895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60087434..60264332hg38UCSC Ensembl
Innerchr3:60073160..60250060hg19UCSC Ensembl
Innerchr3:60048200..60225100hg18UCSC Ensembl
Innerchr3:60048200..60225100hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38176899
hg19176901
hg18176901
hg17176901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752010
Supporting Variants
SamplesSPC_113
Known GenesFHIT
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6990092
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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