A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184841



Internal ID20751881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131036503..131371877hg38UCSC Ensembl
chr11:130906398..131241772hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38335375
hg19335375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6459237
Supporting Variants
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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