A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16987207



Internal ID58914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71723753..71723766hg38UCSC Ensembl
chr6:72433456..72433469hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5395753
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16987207
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.011261


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