A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580228



Internal ID20953299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102162266..102175170hg38UCSC Ensembl
chr10:103922023..103934927hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3812905
hg1912905
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230238
Samples
Known GenesNOLC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580228
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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