A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988014



Internal ID12978739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961836..22264652hg38UCSC Ensembl
Innerchr15:20167089..22552603hg19UCSC Ensembl
Innerchr15:18427103..20053967hg18UCSC Ensembl
Innerchr15:18427103..20053967hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382302817
hg192385515
hg181626865
hg171626865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751387
Supporting Variants
SamplesNA11993
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
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988014
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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