A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16984982



Internal ID57377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87353310..87353361hg38UCSC Ensembl
chr6:88063028..88063079hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394089
Supporting Variants
Samples
Known GenesC6orf163
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16984982
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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