A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024073



Internal ID21933416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:80786294..80795121hg38UCSC Ensembl
chr12:81180073..81188900hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg388828
hg198828
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600749
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024073
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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