A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16978153



Internal ID52838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11978586..11978603hg38UCSC Ensembl
chr6:11978819..11978836hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5551612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16978153
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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