A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647669



Internal ID7034409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35673581..35676865hg38UCSC Ensembl
Innerchr22:35673586..35676861hg38UCSC Ensembl
Outerchr22:35673577..35676870hg38UCSC Ensembl
chr22:36069628..36072912hg19UCSC Ensembl
Innerchr22:36069633..36072908hg19UCSC Ensembl
Outerchr22:36069624..36072917hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg383285
hg193285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16413256
SamplesNA19114
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647669
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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