A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589190



Internal ID20962261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38742443..38745905hg38UCSC Ensembl
chr13:39316580..39320042hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg383463
hg193463
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221815
Samples
Known GenesFREM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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