A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785750



Internal ID18816376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14173029..14181709hg38UCSC Ensembl
Innerchr21:15545350..15554030hg19UCSC Ensembl
Innerchr21:14467221..14475901hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg388681
hg198681
hg188681
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893372
Supporting Variants
Samples
Known GenesLIPI
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785750
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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