A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485786



Internal ID21143339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:114516480..114668933hg38UCSC Ensembl
chr12:114954285..115106738hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38152454
hg19152454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195894
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485786
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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