A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647757



Internal ID7034496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39042894..39047430hg38UCSC Ensembl
Innerchr22:39042927..39047398hg38UCSC Ensembl
Outerchr22:39042862..39047463hg38UCSC Ensembl
chr22:39438899..39443435hg19UCSC Ensembl
Innerchr22:39438932..39443403hg19UCSC Ensembl
Outerchr22:39438867..39443468hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384537
hg194537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16427695, essv16427696
SamplesHG03945, HG00110
Known GenesAPOBEC3F
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647757
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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