A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16915018



Internal ID10768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65315172..65315208hg38UCSC Ensembl
chr2:65542306..65542342hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5394534
Supporting Variants
Samples
Known GenesSPRED2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16915018
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.023091


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