A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358066



Internal ID21015619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177827028..177827398hg38UCSC Ensembl
chr3:177544816..177545186hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358066
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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