A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609551



Internal ID20982622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127624017..127723631hg38UCSC Ensembl
chr6:127945162..128044776hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3899615
hg1999615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215526
Samples
Known GenesTHEMIS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609551
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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