A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893372



Internal ID18837506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14173029..14181709hg38UCSC Ensembl
Outerchr21:14173029..14181709hg38UCSC Ensembl
Innerchr21:15545350..15554030hg19UCSC Ensembl
Outerchr21:15545350..15554030hg19UCSC Ensembl
Innerchr21:14467221..14475901hg18UCSC Ensembl
Outerchr21:14467221..14475901hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg388681
hg198681
hg188681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785750
Samples
Known GenesLIPI
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893372
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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