A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18164194



Internal ID20731235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119758460..119758845hg38UCSC Ensembl
chr8:120770700..120771085hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419867
Supporting Variants
Samples
Known GenesTAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18164194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00167


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