A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893361



Internal ID19184181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10663711..10754646hg38UCSC Ensembl
Outerchr21:10631001..10804226hg38UCSC Ensembl
Innerchr21:10757811..10848746hg19UCSC Ensembl
Outerchr21:10708231..10881456hg19UCSC Ensembl
Innerchr21:9779682..9870617hg18UCSC Ensembl
Outerchr21:9730102..9903327hg18UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38173226
hg19173226
hg18173226
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790090, essv25790013, essv25786842, essv25787270, essv25790476, essv25790851, essv25787334, essv25792084, essv25790119, essv25799168, essv25786822, essv25790139, essv25792351, essv25779239, essv25779111, essv25790124, essv25791760, essv25779179, essv25786832, essv25792371, essv25787529, essv25792273, essv25790070, essv25792448, essv25791702, essv25792357, essv25791748
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893361
Frequency
Sample Size3017
Observed Gain17
Observed Loss10
Observed Complex0
Frequencyn/a


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