A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460774



Internal ID238745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56189774..56197613hg38UCSC Ensembl
chr5:55485601..55493440hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg387840
hg197840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16965512
Samples
Known GenesANKRD55
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460774
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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