A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987618



Internal ID12977161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26345274..26381978hg38UCSC Ensembl
Innerchr3:26386765..26423469hg19UCSC Ensembl
Innerchr3:26361769..26398473hg18UCSC Ensembl
Innerchr3:26361769..26398473hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3836705
hg1936705
hg1836705
hg1736705
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751997
Supporting Variants
SamplesBEC_717
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987618
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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