A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579354



Internal ID20952425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103178676..103179099hg38UCSC Ensembl
chr10:104938433..104938856hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38424
hg19424
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218251
Samples
Known GenesNT5C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579354
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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