A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983943



Internal ID12977428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21757835..22156962hg38UCSC Ensembl
Innerchr3:21799327..22198454hg19UCSC Ensembl
Innerchr3:21774331..22173458hg18UCSC Ensembl
Innerchr3:21774331..22173458hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38399128
hg19399128
hg18399128
hg17399128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751992
Supporting Variants
SamplesBEC_736
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983943
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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