A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500793



Internal ID20874021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14172064..14172549hg38UCSC Ensembl
chr16:14265921..14266406hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028447
Samples
Known GenesMKL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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