A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219768



Internal ID20786808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77962858..78137431hg38UCSC Ensembl
chr8:78875093..79049666hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38174574
hg19174574
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417252
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219768
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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