A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16920292



Internal ID14308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161883154..161883205hg38UCSC Ensembl
chr2:162739664..162739715hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5411448
Supporting Variants
Samples
Known GenesSLC4A10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16920292
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001405


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