A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983730



Internal ID12629144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:145773359..145969518hg38UCSC Ensembl
Innerchr3:145491146..145687305hg19UCSC Ensembl
Innerchr3:146973836..147169995hg18UCSC Ensembl
Innerchr3:146973844..147170003hg17UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38196160
hg19196160
hg18196160
hg17196160
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983730
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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