A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196614



Internal ID20763654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:50737940..50739277hg38UCSC Ensembl
chr18:48264310..48265647hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg381338
hg191338
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6522682
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196614
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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