A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586024



Internal ID20959095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52441110..52442763hg38UCSC Ensembl
chr13:53015245..53016898hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381654
hg191654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219784
Samples
Known GenesVPS36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586024
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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