A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178836



Internal ID20745876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59206737..59250676hg38UCSC Ensembl
chr18:56873969..56917908hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3843940
hg1943940
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520348
Supporting Variants
Samples
Known GenesGRP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178836
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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