A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987887



Internal ID12982378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961836..22198726hg38UCSC Ensembl
Innerchr15:20167089..22486677hg19UCSC Ensembl
Innerchr15:18427103..19988041hg18UCSC Ensembl
Innerchr15:18427103..19988041hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382236891
hg192319589
hg181560939
hg171560939
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34366
Supporting Variants
SamplesNA19159
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)essv6987887
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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