A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441951



Internal ID21099504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125769645..125801934hg38UCSC Ensembl
chr9:128531924..128564213hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3832290
hg1932290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233124
Samples
Known GenesPBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441951
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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