A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140722



Internal ID20707762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25987524..25989403hg38UCSC Ensembl
chr6:25987752..25989631hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg381880
hg191880
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410968
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140722
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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