A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218222



Internal ID20785262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106027899..106039269hg38UCSC Ensembl
chr8:107040127..107051497hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3811371
hg1911371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218222
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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