A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484459



Internal ID21142012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:119194866..119203937hg38UCSC Ensembl
chr12:119632671..119641742hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg389072
hg199072
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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