A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16985820



Internal ID57956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84846573..84846624hg38UCSC Ensembl
chr6:85556291..85556342hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5413373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16985820
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001406


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