A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16910446



Internal ID7734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30901959..30909669hg38UCSC Ensembl
chr2:31124825..31132535hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg387711
hg197711
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5438628
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16910446
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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