A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16921725



Internal ID15256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161006921..161012813hg38UCSC Ensembl
chr2:161863432..161869324hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg385893
hg195893
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5441069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16921725
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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