A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358344



Internal ID21015897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132469801..132472400hg38UCSC Ensembl
chr3:132188645..132191244hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208974
Samples
Known GenesDNAJC13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358344
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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