A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35065



Internal ID12991101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403659..75590759hg38UCSC Ensembl
Innerchr3:75452810..75639910hg19UCSC Ensembl
Innerchr3:75535500..75722600hg18UCSC Ensembl
Innerchr3:75535500..75722600hg17UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38187101
hg19187101
hg18187101
hg17187101
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv180e55
Supporting Variantsessv6989059, essv6979036, essv6988086, essv6979037
SamplesNA12864
Known GenesFAM86DP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35065
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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