A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043581



Internal ID21952875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48346138..48346207hg38UCSC Ensembl
chr22:48741950..48742019hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043581
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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