A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580088



Internal ID20953159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102701946..102702613hg38UCSC Ensembl
chr13:103354296..103354963hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580088
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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