A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361104



Internal ID21018657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167177548..167188264hg38UCSC Ensembl
chr3:166895336..166906052hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3810717
hg1910717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361104
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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