A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785311



Internal ID19177534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:140028857..140035807hg38UCSC Ensembl
Innerchr8:141038954..141045904hg19UCSC Ensembl
Innerchr8:141108136..141115086hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg386951
hg196951
hg186951
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891494
Supporting Variants
Samples
Known GenesTRAPPC9
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785311
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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