A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002107



Internal ID20569147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62615225..62615626hg38UCSC Ensembl
chr12:63009005..63009406hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468951
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00082


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