A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786832



Internal ID19160302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10663711..10784632hg38UCSC Ensembl
Innerchr21:10727825..10848746hg19UCSC Ensembl
Innerchr21:9749696..9870617hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38120922
hg19120922
hg18120922
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893361
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786832
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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