A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191297



Internal ID20758337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:90557352..90819825hg38UCSC Ensembl
chr12:90951129..91213602hg19UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38262474
hg19262474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191297
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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