A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223393



Internal ID20790433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:38509054..38542691hg38UCSC Ensembl
chr6:38476830..38510467hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3833638
hg1933638
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405109
Supporting Variants
Samples
Known GenesBTBD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223393
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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