A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592387



Internal ID20965458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103305353..103307094hg38UCSC Ensembl
chr10:105065110..105066851hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg381742
hg191742
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv877n223
Supporting Variantsnssv18232636
Samples
Known GenesPCGF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592387
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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