A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576067



Internal ID20949138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36637775..36638835hg38UCSC Ensembl
chr13:37211912..37212972hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381061
hg191061
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576067
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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