A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5468931



Internal ID246724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136544931..136551564hg38UCSC Ensembl
chr5:135880620..135887253hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg386634
hg196634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974431
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5468931
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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