A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569755



Internal ID20942826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127595629..127596396hg38UCSC Ensembl
chr9:130357908..130358675hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7943n223
Supporting Variantsnssv18279955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569755
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