A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590951



Internal ID20964022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106855026..106855465hg38UCSC Ensembl
chr13:107507374..107507813hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38440
hg19440
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590951
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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