A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623764



Internal ID7010620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70368166..70371149hg38UCSC Ensembl
Innerchr10:70368216..70371099hg38UCSC Ensembl
Outerchr10:70368116..70371199hg38UCSC Ensembl
chr10:72127922..72130905hg19UCSC Ensembl
Innerchr10:72127972..72130855hg19UCSC Ensembl
Outerchr10:72127872..72130955hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382984
hg192984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13858617
SamplesHG01991
Known GenesLRRC20
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623764
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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