A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192988



Internal ID20760029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107589747..108030232hg38UCSC Ensembl
chr11:107460473..107900958hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38440486
hg19440486
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456840
Supporting Variants
Samples
Known GenesCUL5, ELMOD1, LOC643923, RAB39A, SLC35F2, SLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192988
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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