A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164446



Internal ID20731486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:120913043..120913494hg38UCSC Ensembl
chr8:121925283..121925734hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00063


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