A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193807



Internal ID20760847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87763200..87801575hg38UCSC Ensembl
chr13:88415455..88453830hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3838376
hg1938376
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6479877
Supporting Variants
Samples
Known GenesLINC00397
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193807
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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