A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214573



Internal ID20781614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120924901..120930600hg38UCSC Ensembl
chr6:121246047..121251746hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604578
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00056


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