A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216919



Internal ID20783959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:14283378..14302033hg38UCSC Ensembl
chr6:14283609..14302264hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3818656
hg1918656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396058
Supporting Variants
Samples
Known GenesLINC01108
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216919
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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