A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590095



Internal ID20963166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29944407..29944899hg38UCSC Ensembl
chr13:30518544..30519036hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219900
Samples
Known GenesLINC00544
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590095
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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