A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367028



Internal ID21024581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133410702..133465342hg38UCSC Ensembl
chr3:133129546..133184186hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3854641
hg1954641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094793
Samples
Known GenesBFSP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367028
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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