A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799386



Internal ID18819466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:16442717..16561877hg38UCSC Ensembl
Innerchr21:17815037..17934197hg19UCSC Ensembl
Innerchr21:16736908..16856068hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38119161
hg19119161
hg18119161
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893374
Supporting Variants
Samples
Known GenesLINC00478, MIR99A, MIRLET7C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799386
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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