A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458154



Internal ID21115707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102021446..102022073hg38UCSC Ensembl
chr12:102415224..102415851hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg38628
hg19628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996736
Samples
Known GenesCCDC53
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458154
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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