A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280018



Internal ID20847058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129607011..129820589hg38UCSC Ensembl
chr9:132369290..132582868hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38213579
hg19213579
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573040
Supporting Variants
Samples
Known GenesASB6, C9orf50, NTMT1, PRRX2, PTGES, TOR1A, TOR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280018
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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