A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216851



Internal ID20783891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13765322..13776347hg38UCSC Ensembl
chr6:13765554..13776579hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3811026
hg1911026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403285
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216851
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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