A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073628



Internal ID20640668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33674372..33709761hg38UCSC Ensembl
chr22:34070358..34105747hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3835390
hg1935390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554953
Supporting Variants
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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