A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16971319



Internal ID48223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:90270931..90271310hg38UCSC Ensembl
chr5:89566748..89567127hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5471488
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16971319
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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