A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457655



Internal ID235695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28640493..28728389hg38UCSC Ensembl
chr5:28640600..28728496hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3887897
hg1987897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16964035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457655
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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