A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074206



Internal ID20641246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34753701..34777600hg38UCSC Ensembl
chr22:35149692..35173591hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3823900
hg1923900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550478
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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