A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368809



Internal ID21026362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:133869679..133870169hg38UCSC Ensembl
chr3:133588523..133589013hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094807
Samples
Known GenesRAB6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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