A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027392



Internal ID21936735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114624462..114624879hg38UCSC Ensembl
chr12:115062267..115062684hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38418
hg19418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027392
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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