A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987908



Internal ID12972778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051935..4092560hg38UCSC Ensembl
Innerchr3:4093619..4134244hg19UCSC Ensembl
Innerchr3:4068619..4109244hg18UCSC Ensembl
Innerchr3:4068619..4109244hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3840626
hg1940626
hg1840626
hg1740626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752005
Supporting Variants
SamplesBEC_350
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987908
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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