A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909517



Internal ID7124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14381746..14426894hg38UCSC Ensembl
chr2:14521870..14567018hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3845149
hg1945149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446722
Supporting Variants
Samples
Known GenesLINC00276
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909517
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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