A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182568



Internal ID20749608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127542825..127543164hg38UCSC Ensembl
chr11:127412720..127413059hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182568
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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