A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334389



Internal ID20867574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:74184701..74198100hg38UCSC Ensembl
chr1:74650385..74663784hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv241n223
Supporting Variantsnssv18204407
Samples
Known GenesLRRIQ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334389
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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