A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996107



Internal ID20563147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106276984..106277595hg38UCSC Ensembl
chr12:106670762..106671373hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996107
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01635


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