A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163429



Internal ID20730469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114783785..114784382hg38UCSC Ensembl
chr8:115796014..115796611hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427519
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163429
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00077


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