A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074319



Internal ID20641359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34663398..34675376hg38UCSC Ensembl
chr22:35059390..35071367hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3811979
hg1911978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543107
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074319
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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