A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456563



Internal ID234626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:78865952..78866009hg38UCSC Ensembl
chr6:79575669..79575726hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456563
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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