A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192971



Internal ID20760011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60609601..60626600hg38UCSC Ensembl
chr11:60377074..60394073hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3817000
hg1917000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457245
Supporting Variants
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192971
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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