A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979477



Internal ID53700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9523547..9535484hg38UCSC Ensembl
chr6:9523780..9535717hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3811938
hg1911938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979477
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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