A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587603



Internal ID20960674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25306193..25307195hg38UCSC Ensembl
chr13:25880331..25881333hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381003
hg191003
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224152
Samples
Known GenesNUPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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