A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187871



Internal ID20754911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72355538..72356037hg38UCSC Ensembl
chr11:72066582..72067081hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465634
Supporting Variants
Samples
Known GenesCLPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187871
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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