A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484157



Internal ID21141710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113755029..113760949hg38UCSC Ensembl
chr12:114192834..114198754hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg385921
hg195921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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