A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368068



Internal ID21025621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179450001..179452000hg38UCSC Ensembl
chr3:179167789..179169788hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211517
Samples
Known GenesGNB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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