A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16963849



Internal ID43209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26479437..26481917hg38UCSC Ensembl
chr5:26479546..26482026hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg382481
hg192481
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462776
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16963849
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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