A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180468



Internal ID20747508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20879987..21208515hg38UCSC Ensembl
chr13:21454126..21782654hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38328529
hg19328529
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488882
Supporting Variants
Samples
Known GenesLATS2, LINC00367, MRP63, SAP18, SKA3, XPO4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180468
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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