A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784819



Internal ID18817464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42965277..43092949hg38UCSC Ensembl
Innerchr15:43257475..43385147hg19UCSC Ensembl
Innerchr15:41044767..41172439hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38127673
hg19127673
hg18127673
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892680
Supporting Variants
Samples
Known GenesUBR1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=17
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784819
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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