A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985173



Internal ID12982902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60103588..60290993hg38UCSC Ensembl
Innerchr3:60089314..60276722hg19UCSC Ensembl
Innerchr3:60064354..60251762hg18UCSC Ensembl
Innerchr3:60064354..60251762hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38187406
hg19187409
hg18187409
hg17187409
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985173
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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