A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222406



Internal ID20789446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8355868..8817527hg38UCSC Ensembl
chr8:8213384..8675037hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38461660
hg19461654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6424190
Supporting Variants
Samples
Known GenesCLDN23, MFHAS1, SGK223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222406
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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