A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799361



Internal ID19174568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1175210..1181971hg38UCSC Ensembl
Innerchr20:1155854..1162615hg19UCSC Ensembl
Innerchr20:1103854..1110615hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386762
hg196762
hg186762
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893267
Supporting Variants
Samples
Known GenesTMEM74B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799361
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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