A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778718



Internal ID18819546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14874289..14886776hg38UCSC Ensembl
Innerchr20:14854935..14867422hg19UCSC Ensembl
Innerchr20:14802935..14815422hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3812488
hg1912488
hg1812488
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893313
Supporting Variants
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778718
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer