A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231749



Internal ID20798789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82067101..82207552hg38UCSC Ensembl
chr8:82979336..83119787hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38140452
hg19140452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432556
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231749
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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