A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16963871



Internal ID43226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26741041..26741610hg38UCSC Ensembl
chr5:26741150..26741719hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16963871
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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