A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617051



Internal ID20990122
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 StatusM
Merged Variants
Supporting Variantsnssv18215584
Samples
Known GenesTAAR1, TAAR2, VNN1, VNN2, VNN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617051
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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