A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995986



Internal ID20563026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105767946..105768423hg38UCSC Ensembl
chr12:106161724..106162201hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462016
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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