A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163025



Internal ID20730067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111343270..111443665hg38UCSC Ensembl
chr8:112355499..112455894hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38100396
hg19100396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426953
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163025
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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