A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215584



Internal ID20782624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132613927..132764581hg38UCSC Ensembl
chr6:132935066..133085720hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38150655
hg19150655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617051
Supporting Variants
Samples
Known GenesTAAR1, TAAR2, VNN1, VNN2, VNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215584
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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