A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989388



Internal ID12629149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145755233..146040407hg38UCSC Ensembl
Innerchr3:145473020..145758194hg19UCSC Ensembl
Innerchr3:146955710..147240884hg18UCSC Ensembl
Innerchr3:146955718..147240892hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38285175
hg19285175
hg18285175
hg17285175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751980
Supporting Variants
SamplesBEC_618
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989388
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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