A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214529



Internal ID20781569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116462601..116468200hg38UCSC Ensembl
chr6:116783764..116789363hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617620
Supporting Variants
Samples
Known GenesFAM26F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00059


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