A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6986025



Internal ID12635962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20246097..22264652hg38UCSC Ensembl
Innerchr15:20451350..22552603hg19UCSC Ensembl
Innerchr15:18711364..20053967hg18UCSC Ensembl
Innerchr15:18711364..20053967hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382018556
hg192101254
hg181342604
hg171342604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751471
Supporting Variants
SamplesNA19210
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)essv6986025
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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