A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988200



Internal ID12980401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20246097..22270557hg38UCSC Ensembl
Innerchr15:20451350..22558508hg19UCSC Ensembl
Innerchr15:18711364..20059872hg18UCSC Ensembl
Innerchr15:18711364..20059872hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382024461
hg192107159
hg181348509
hg171348509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34909
Supporting Variants
SamplesNA18572
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)essv6988200
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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