A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142426



Internal ID20709466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166081401..166088800hg38UCSC Ensembl
chr6:166494889..166502288hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613388
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00818


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