A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542325



Internal ID20915589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25766221..25767012hg38UCSC Ensembl
chr3:25807712..25808503hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38792
hg19792
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4825n223
Supporting Variantsnssv18262618
Samples
Known GenesNGLY1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542325
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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