A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199872



Internal ID20766912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20596289..20618782hg38UCSC Ensembl
chr1:20922782..20945275hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3822494
hg1922494
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318561
Supporting Variants
Samples
Known GenesCDA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199872
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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