A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201927



Internal ID20768968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165043715..165056898hg38UCSC Ensembl
chr1:165012952..165026135hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3813184
hg1913184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324446
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201927
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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