A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622390



Internal ID6662560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12910191..12914490hg38UCSC Ensembl
Innerchr10:12910191..12914490hg38UCSC Ensembl
Outerchr10:12909691..12914990hg38UCSC Ensembl
chr10:12952191..12956490hg19UCSC Ensembl
Innerchr10:12952191..12956490hg19UCSC Ensembl
Outerchr10:12951691..12956990hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13697834, essv13697835
SamplesHG01497, HG01498
Known GenesCCDC3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622390
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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