A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592490



Internal ID20965561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100228357..100228668hg38UCSC Ensembl
chr13:100880611..100880922hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228306
Samples
Known GenesPCCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592490
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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