A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373337



Internal ID21030890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32816001..32821600hg38UCSC Ensembl
chr3:32857493..32863092hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4833n223
Supporting Variantsnssv18210530
Samples
Known GenesTRIM71
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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