A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473093



Internal ID21130646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:66959199..67050398hg38UCSC Ensembl
chr12:67352979..67444178hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg3891200
hg1991200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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