A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214583



Internal ID20781624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121465427..121470563hg38UCSC Ensembl
chr6:121786573..121791709hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385137
hg195137
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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