A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17642957



Internal ID21835004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42719285..42719285hg38UCSC Ensembl
chr22:43115291..43115291hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111230
Supporting Variants
Samples
Known GenesA4GALT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17642957
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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