A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232033



Internal ID20799073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26890769..27001680hg38UCSC Ensembl
chr8:26748286..26859197hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38110912
hg19110912
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427253
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232033
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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