A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465554



Internal ID21123107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105446616..105453058hg38UCSC Ensembl
chr12:105840394..105846836hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg386443
hg196443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995970
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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