A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182481



Internal ID20749521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13550633..13551045hg38UCSC Ensembl
chr18:13550632..13551044hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521908
Supporting Variants
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182481
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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