A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201814



Internal ID20768855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201981202..201992247hg38UCSC Ensembl
chr1:201950330..201961375hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3811046
hg1911046
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322570
Supporting Variants
Samples
Known GenesRNPEP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201814
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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