A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18199852



Internal ID20766892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19337854..19351484hg38UCSC Ensembl
chr1:19664348..19677978hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3813631
hg1913631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321058
Supporting Variants
Samples
Known GenesCAPZB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18199852
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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