A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965546



Internal ID44352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56563947..56564009hg38UCSC Ensembl
chr5:55859774..55859836hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457560
Supporting Variants
Samples
Known GenesLOC101928448
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965546
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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