A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592381



Internal ID20965452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36688361..36689251hg38UCSC Ensembl
chr13:37262498..37263388hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225804
Samples
Known GenesSERTM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592381
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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