A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216068



Internal ID20783108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167972601..168316300hg38UCSC Ensembl
chr6:168373281..168716980hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38343700
hg19343700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611382
Supporting Variants
Samples
Known GenesDACT2, FRMD1, HGC6.3, KIF25, KIF25-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01141


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