A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457741



Internal ID235779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96464773..96474173hg38UCSC Ensembl
chr5:95800477..95809877hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg389401
hg199401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457741
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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