A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965545



Internal ID44351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56562404..56562517hg38UCSC Ensembl
chr5:55858231..55858344hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460936
Supporting Variants
Samples
Known GenesLOC101928448
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965545
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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