A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981975



Internal ID12627544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051935..4198163hg38UCSC Ensembl
Innerchr3:4093619..4239847hg19UCSC Ensembl
Innerchr3:4068619..4214847hg18UCSC Ensembl
Innerchr3:4068619..4214847hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38146229
hg19146229
hg18146229
hg17146229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752006
Supporting Variants
SamplesBEC_51
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981975
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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