A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216679



Internal ID20783719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155029648..155136406hg38UCSC Ensembl
chr6:155350782..155457540hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg38106759
hg19106759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619307
Supporting Variants
Samples
Known GenesTIAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216679
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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