A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356288



Internal ID21013841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:125349201..125390900hg38UCSC Ensembl
chr3:125068045..125109744hg19UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg3841700
hg1941700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208422
Samples
Known GenesZNF148
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356288
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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