A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965606



Internal ID44386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54575531..54576949hg38UCSC Ensembl
chr5:53871361..53872779hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381419
hg191419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965606
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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