A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583532



Internal ID20956603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27438383..27438663hg38UCSC Ensembl
chr13:28012520..28012800hg19UCSC Ensembl
Cytoband13q12.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224195
Samples
Known GenesMTIF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583532
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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