A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645348



Internal ID21837395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38060049..38061179hg38UCSC Ensembl
chr22:38456056..38457186hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6055211
Supporting Variants
Samples
Known GenesPICK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645348
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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