A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574246



Internal ID20947317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:686466..862371hg38UCSC Ensembl
chr9:686466..862371hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38175906
hg19175906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280809
Samples
Known GenesDMRT1, KANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574246
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