A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609228



Internal ID20982299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121269446..121287360hg38UCSC Ensembl
chr6:121590592..121608506hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3817915
hg1917915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214581
Samples
Known GenesTBC1D32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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