A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193526



Internal ID20760566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130720235..131215048hg38UCSC Ensembl
chr11:130590130..131084943hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38494814
hg19494814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467171
Supporting Variants
Samples
Known GenesSNX19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193526
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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