A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624818



Internal ID7011668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124798048..124800903hg38UCSC Ensembl
Innerchr10:124798048..124800903hg38UCSC Ensembl
Outerchr10:124797929..124801036hg38UCSC Ensembl
chr10:126486617..126489472hg19UCSC Ensembl
Innerchr10:126486617..126489472hg19UCSC Ensembl
Outerchr10:126486498..126489605hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382856
hg192856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963337, essv13963336, essv13963341, essv13963340, essv13963339, essv13963342, essv13963338
SamplesNA19314, NA19026, NA19776, HG02817, HG02839, NA20797, NA19475
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624818
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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