A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991110



Internal ID61480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160915415..160915415hg38UCSC Ensembl
chr6:161336447..161336447hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38271
hg19271
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5540678
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991110
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.138302


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