A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042356



Internal ID21951673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42192165..42192396hg38UCSC Ensembl
chr22:42588171..42588402hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648172
Samples
Known GenesTCF20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042356
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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