A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978071



Internal ID12978589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20246097..22160801hg38UCSC Ensembl
Innerchr15:20451350..22448752hg19UCSC Ensembl
Innerchr15:18711364..19950116hg18UCSC Ensembl
Innerchr15:18711364..19950116hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381914705
hg191997403
hg181238753
hg171238753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751445
Supporting Variants
SamplesNA11829
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)essv6978071
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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