A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191821



Internal ID20758861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31753901..31754900hg38UCSC Ensembl
chr13:32328038..32329037hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492739
Supporting Variants
Samples
Known GenesRXFP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191821
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0839


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