A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170897



Internal ID20737937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8695445..8757576hg38UCSC Ensembl
chr8:8552955..8615086hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3862132
hg1962132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423410
Supporting Variants
Samples
Known GenesCLDN23
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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