A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369200



Internal ID21026753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28347801..28349500hg38UCSC Ensembl
chr3:28389292..28390991hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210481
Samples
Known GenesAZI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369200
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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