A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588656



Internal ID20961727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30265754..30266113hg38UCSC Ensembl
chr13:30839891..30840250hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227154
Samples
Known GenesKATNAL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588656
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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