A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980233



Internal ID12981487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20246097..22155980hg38UCSC Ensembl
Innerchr15:20451350..22443931hg19UCSC Ensembl
Innerchr15:18711364..19945295hg18UCSC Ensembl
Innerchr15:18711364..19945295hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381909884
hg191992582
hg181233932
hg171233932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751388
Supporting Variants
SamplesNA18971
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980233
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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