A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16986885



Internal ID58700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92354025..92443632hg38UCSC Ensembl
chr6:93063743..93153350hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3889608
hg1989608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470829
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16986885
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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