A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2751413



Internal ID12984965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961836..22300068hg38UCSC Ensembl
Innerchr15:20167089..22588019hg19UCSC Ensembl
Innerchr15:18427103..20089383hg18UCSC Ensembl
Innerchr15:18427103..20089383hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382338233
hg192420931
hg181662281
hg171662281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv96e55
Supporting Variantsessv6984690, essv6984691
SamplesSPC_166
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
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)esv2751413
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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