A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25793660



Internal ID19175417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13793448..13843493hg38UCSC Ensembl
Innerchr21:15165769..15215814hg19UCSC Ensembl
Innerchr21:14087640..14137685hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3850046
hg1950046
hg1850046
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893366
Supporting Variants
Samples
Known GenesC21orf15
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=12
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25793660
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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