A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980725



Internal ID54529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19319115..19319289hg38UCSC Ensembl
chr6:19319346..19319520hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140879
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980725
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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