A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647806



Internal ID7034545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41955157..41961379hg38UCSC Ensembl
Innerchr22:41955657..41960879hg38UCSC Ensembl
Outerchr22:41954157..41962379hg38UCSC Ensembl
chr22:42351161..42357383hg19UCSC Ensembl
Innerchr22:42351661..42356883hg19UCSC Ensembl
Outerchr22:42350161..42358383hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg386223
hg196223
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16430354
SamplesNA20795
Known GenesLINC00634
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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