A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996844



Internal ID20563884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:113409930..113410877hg38UCSC Ensembl
chr12:113847735..113848682hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38948
hg19948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493606
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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