A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623664



Internal ID7010520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66965958..66973053hg38UCSC Ensembl
Innerchr10:66966458..66972553hg38UCSC Ensembl
Outerchr10:66964958..66974053hg38UCSC Ensembl
chr10:68725716..68732811hg19UCSC Ensembl
Innerchr10:68726216..68732311hg19UCSC Ensembl
Outerchr10:68724716..68733811hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg387096
hg197096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13844618, essv13844617
SamplesHG03175, NA19309
Known GenesCTNNA3, LRRTM3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623664
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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