A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479237



Internal ID21136790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:116697307..116702249hg38UCSC Ensembl
chr12:117135112..117140054hg19UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg384943
hg194943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997162
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479237
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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