A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074514



Internal ID20641554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41520608..41535702hg38UCSC Ensembl
chr22:41916612..41931706hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3815095
hg1915095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551307
Supporting Variants
Samples
Known GenesACO2, POLR3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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