A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6579636



Internal ID20952707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90540794..90540924hg38UCSC Ensembl
chr13:91193048..91193178hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226630
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6579636
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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