A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622764



Internal ID7009622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29082942..29296501hg38UCSC Ensembl
Innerchr10:29083092..29296351hg38UCSC Ensembl
Outerchr10:29082792..29296651hg38UCSC Ensembl
chr10:29371871..29585430hg19UCSC Ensembl
Innerchr10:29372021..29585280hg19UCSC Ensembl
Outerchr10:29371721..29585580hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38213560
hg19213560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13742667
SamplesNA19236
Known GenesLYZL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622764
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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