A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16911359



Internal ID8337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28835640..28835691hg38UCSC Ensembl
chr2:29058506..29058557hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5403630
Supporting Variants
Samples
Known GenesSPDYA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16911359
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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