A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784597



Internal ID19163756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13964098..14028297hg38UCSC Ensembl
Innerchr21:15336419..15400618hg19UCSC Ensembl
Innerchr21:14258290..14322489hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3864200
hg1964200
hg1864200
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893369
Supporting Variants
Samples
Known GenesANKRD20A11P
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784597
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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