A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140239



Internal ID20707279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:143547671..143555567hg38UCSC Ensembl
chr6:143868808..143876704hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387897
hg197897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606596
Supporting Variants
Samples
Known GenesLOC285740
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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