A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201898



Internal ID20768939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162611756..162614382hg38UCSC Ensembl
chr1:162581546..162584172hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382627
hg192627
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330607
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00846


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