A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369155



Internal ID21026708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95811931..95818903hg38UCSC Ensembl
chr3:95530775..95537747hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg386973
hg196973
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369155
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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