A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622339



Internal ID6662509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11478380..11480469hg38UCSC Ensembl
Innerchr10:11478383..11480466hg38UCSC Ensembl
Outerchr10:11478377..11480472hg38UCSC Ensembl
chr10:11520379..11522468hg19UCSC Ensembl
Innerchr10:11520382..11522465hg19UCSC Ensembl
Outerchr10:11520376..11522471hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382090
hg192090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13695985, essv13695984
SamplesNA18986, NA18994
Known GenesUSP6NL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622339
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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