A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988086



Internal ID12979528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403659..75416959hg38UCSC Ensembl
Innerchr3:75452810..75466110hg19UCSC Ensembl
Innerchr3:75535500..75548800hg18UCSC Ensembl
Innerchr3:75535500..75548800hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3813301
hg1913301
hg1813301
hg1713301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35065
Supporting Variants
SamplesNA12864
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988086
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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