A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17996927



Internal ID20563967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110605901..110611500hg38UCSC Ensembl
chr12:111043706..111049305hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486183
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17996927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0028


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