A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987891



Internal ID12982398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20246097..22253153hg38UCSC Ensembl
Innerchr15:20451350..22541104hg19UCSC Ensembl
Innerchr15:18711364..20042468hg18UCSC Ensembl
Innerchr15:18711364..20042468hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382007057
hg192089755
hg181331105
hg171331105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751444
Supporting Variants
SamplesNA19161
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)essv6987891
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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