A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460768



Internal ID21118321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104796883..104797316hg38UCSC Ensembl
chr12:105190661..105191094hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38434
hg19434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995929
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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