A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184192



Internal ID20751232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52302601..52334200hg38UCSC Ensembl
chr13:52876736..52908335hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg3831600
hg1931600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492323
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00226


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