A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456714



Internal ID234775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177625445..177626293hg38UCSC Ensembl
chr5:177052446..177053294hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38849
hg19849
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976823
Samples
Known GenesLOC202181
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456714
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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