A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799516



Internal ID19165389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140025266..140044486hg38UCSC Ensembl
Innerchr8:141035363..141054583hg19UCSC Ensembl
Innerchr8:141104545..141123765hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3819221
hg1919221
hg1819221
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891493
Supporting Variants
Samples
Known GenesTRAPPC9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799516
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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