A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983519



Internal ID12976423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961836..22300068hg38UCSC Ensembl
Innerchr15:20167089..22588019hg19UCSC Ensembl
Innerchr15:18427103..20089383hg18UCSC Ensembl
Innerchr15:18427103..20089383hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382338233
hg192420931
hg181662281
hg171662281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751412
Supporting Variants
SamplesBEC_665
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)essv6983519
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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