A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6378125



Internal ID21035678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126224401..126228000hg38UCSC Ensembl
chr4:127145556..127149155hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6378125
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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