A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592589



Internal ID20965660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40356900..40870021hg38UCSC Ensembl
chr13:40931037..41444157hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38513122
hg19513121
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1808n223
Supporting Variantsnssv18232444
Samples
Known GenesFOXO1, LINC00598, MIR320D1, MIR621, MRPS31, SLC25A15, TPTE2P5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592589
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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