A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573267



Internal ID20946338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99521867..99522449hg38UCSC Ensembl
chr6:99969743..99970325hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272842
Samples
Known GenesTSTD3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573267
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer