A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577370



Internal ID20950441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27112380..27112959hg38UCSC Ensembl
chr13:27686517..27687096hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221430
Samples
Known GenesUSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577370
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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