A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17690628



Internal ID114294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106536836..106536887hg38UCSC Ensembl
chr12:106930614..106930665hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5416242
Supporting Variants
Samples
Known GenesLOC100287944
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17690628
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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