A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592280



Internal ID20965351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96028884..96029316hg38UCSC Ensembl
chr13:96681138..96681570hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223102
Samples
Known GenesUGGT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592280
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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