A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623157



Internal ID6663325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48616895..48621968hg38UCSC Ensembl
Innerchr10:48616928..48621936hg38UCSC Ensembl
Outerchr10:48616863..48622001hg38UCSC Ensembl
chr10:49824940..49830013hg19UCSC Ensembl
Innerchr10:49824973..49829981hg19UCSC Ensembl
Outerchr10:49824908..49830046hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385074
hg195074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796098
SamplesHG03884
Known GenesARHGAP22
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623157
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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