A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484882



Internal ID21142435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:118200842..118201448hg38UCSC Ensembl
chr12:118638647..118639253hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997237
Samples
Known GenesTAOK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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