A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595076



Internal ID20968147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30643619..30644224hg38UCSC Ensembl
chr13:31217756..31218361hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217275
Samples
Known GenesUSPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595076
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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