A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201863



Internal ID20768904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2053263..2055142hg38UCSC Ensembl
chr1:1984702..1986581hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg381880
hg191880
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330084
Supporting Variants
Samples
Known GenesPRKCZ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201863
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00145


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