A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165674



Internal ID20732714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132040586..132049537hg38UCSC Ensembl
chr8:133052833..133061784hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg388952
hg198952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423136
Supporting Variants
Samples
Known GenesOC90
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165674
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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