A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459677



Internal ID237687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153291659..153302000hg38UCSC Ensembl
chr5:152671219..152681560hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3810342
hg1910342
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975700, nssv16975701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459677
Frequency
Sample Size3202
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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