A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783929



Internal ID19177862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:47415238..47469940hg38UCSC Ensembl
Innerchr20:46043982..46098684hg19UCSC Ensembl
Innerchr20:45477389..45532091hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3854703
hg1954703
hg1854703
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893342
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783929
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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