A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477696



Internal ID21135249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113987277..114145761hg38UCSC Ensembl
chr12:114425082..114583566hg19UCSC Ensembl
Cytoband12q24.21
Allele length
AssemblyAllele length
hg38158485
hg19158485
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178356
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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