A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200962



Internal ID20768002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159043301..159047700hg38UCSC Ensembl
chr1:159013091..159017490hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326222
Supporting Variants
Samples
Known GenesIFI16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200962
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01077


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