A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575440



Internal ID20948511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130447009..130450556hg38UCSC Ensembl
chr9:133322396..133325943hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383548
hg193548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280047
Samples
Known GenesASS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575440
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