A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358918



Internal ID21016471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:164304947..165126388hg38UCSC Ensembl
chr3:164022735..164844176hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38821442
hg19821442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208625
Samples
Known GenesSI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358918
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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