A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026477



Internal ID21935820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:67772125..67774532hg38UCSC Ensembl
chr12:68165905..68168312hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg382408
hg192408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606053
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026477
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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