A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463420



Internal ID21120973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:103445329..103453255hg38UCSC Ensembl
chr12:103839107..103847033hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg387927
hg197927
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995643
Samples
Known GenesC12orf42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463420
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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