A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965511



Internal ID44329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56187656..56187861hg38UCSC Ensembl
chr5:55483483..55483688hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459385
Supporting Variants
Samples
Known GenesANKRD55
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965511
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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