A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35069



Internal ID12644419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15666599..15728649hg38UCSC Ensembl
Innerchr19:15777409..15839459hg19UCSC Ensembl
Innerchr19:15638409..15700459hg18UCSC Ensembl
Innerchr19:15638409..15700459hg17UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3862051
hg1962051
hg1862051
hg1762051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv137e55
Supporting Variantsessv6988341, essv6980995, essv6985458, essv6980996, essv6980994
SamplesNA19171
Known GenesCYP4F12, OR10H2
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)esv35069
Frequency
Sample Size771
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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