A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358632



Internal ID21016185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28342643..28364830hg38UCSC Ensembl
chr3:28384134..28406321hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3822188
hg1922188
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210480
Samples
Known GenesAZI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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