A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986219



Internal ID58238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:103513790..103866895hg38UCSC Ensembl
chr6:103961665..104314770hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38353106
hg19353106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986219
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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