A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572200



Internal ID20945271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128606019..128606488hg38UCSC Ensembl
chr9:131368298..131368767hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279986
Samples
Known GenesSPTAN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572200
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