A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496727



Internal ID273796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:129041728..129060000hg38UCSC Ensembl
chr12:129526273..129544545hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3818273
hg1918273
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17685371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496727
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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