A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989059



Internal ID12979518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403668..75590743hg38UCSC Ensembl
Innerchr3:75452819..75639894hg19UCSC Ensembl
Innerchr3:75535509..75722584hg18UCSC Ensembl
Innerchr3:75535509..75722584hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38187076
hg19187076
hg18187076
hg17187076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35065
Supporting Variants
SamplesNA12864
Known GenesFAM86DP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989059
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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