A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487823



Internal ID21145376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114253675..114254327hg38UCSC Ensembl
chr12:114691480..114692132hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38653
hg19653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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