A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279971



Internal ID20847011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128184709..128185196hg38UCSC Ensembl
chr9:130946988..130947475hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564294
Supporting Variants
Samples
Known GenesCIZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279971
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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