A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965541



Internal ID44348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56538412..56538544hg38UCSC Ensembl
chr5:55834239..55834371hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459017
Supporting Variants
Samples
Known GenesLOC101928448
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965541
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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