A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6570274



Internal ID20943345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129538594..129734493hg38UCSC Ensembl
chr9:132300873..132496772hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38195900
hg19195900
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280016
Samples
Known GenesASB6, C9orf50, NTMT1, PRRX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6570274
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