A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508257



Internal ID284952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5016505..5016594hg38UCSC Ensembl
chr12:5125671..5125760hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052774
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508257
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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