A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164084



Internal ID20731124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124779857..124783140hg38UCSC Ensembl
chr8:125792099..125795382hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg383284
hg193284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428561
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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