A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214597



Internal ID20781638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123188520..124009575hg38UCSC Ensembl
chr6:123509665..124330720hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38821056
hg19821056
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608771
Supporting Variants
Samples
Known GenesNKAIN2, TRDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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