A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16918737



Internal ID13267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:110780566..110781163hg38UCSC Ensembl
chr2:111538143..111538740hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5439870
Supporting Variants
Samples
Known GenesACOXL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16918737
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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