A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34622



Internal ID12643972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961836..22122310hg38UCSC Ensembl
Innerchr15:20167089..22410261hg19UCSC Ensembl
Innerchr15:18427103..19911625hg18UCSC Ensembl
Innerchr15:18427103..19911625hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382160475
hg192243173
hg181484523
hg171484523
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv92e55
Supporting Variantsessv6978379, essv6986599
SamplesNA19012
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N4, POTEB, POTEB2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34622
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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