A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165600



Internal ID20732640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144916901..144941800hg38UCSC Ensembl
chr8:146142286..146167186hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3824900
hg1924901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426966
Supporting Variants
Samples
Known GenesZNF16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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