A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623687



Internal ID7010543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67566046..67586751hg38UCSC Ensembl
Innerchr10:67566108..67586689hg38UCSC Ensembl
Outerchr10:67565984..67586813hg38UCSC Ensembl
chr10:69325804..69346509hg19UCSC Ensembl
Innerchr10:69325866..69346447hg19UCSC Ensembl
Outerchr10:69325742..69346571hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3820706
hg1920706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13846274, essv13846275
SamplesNA18749, NA18555
Known GenesCTNNA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623687
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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