A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987689



Internal ID12983542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:66802286..66833686hg38UCSC Ensembl
Innerchr3:66852710..66884110hg19UCSC Ensembl
Innerchr3:66935400..66966800hg18UCSC Ensembl
Innerchr3:66935400..66966800hg17UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3831401
hg1931401
hg1831401
hg1731401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752013
Supporting Variants
SamplesSPC_180
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987689
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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