A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171179



Internal ID20738219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79187212..79187969hg38UCSC Ensembl
chr8:80099447..80100204hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429688
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171179
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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