A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074648



Internal ID20641688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:50771192..50771426hg38UCSC Ensembl
chr22:51209620..51209854hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550044
Supporting Variants
Samples
Known GenesRABL2B, RPL23AP82
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00203


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