A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989549



Internal ID12627548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051528..4197710hg38UCSC Ensembl
Innerchr3:4093212..4239394hg19UCSC Ensembl
Innerchr3:4068212..4214394hg18UCSC Ensembl
Innerchr3:4068212..4214394hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38146183
hg19146183
hg18146183
hg17146183
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989549
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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