A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368161



Internal ID21025714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:128027916..128034381hg38UCSC Ensembl
chr3:127746759..127753224hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg386466
hg196466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208482
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368161
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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