A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280091



Internal ID20847131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132344331..132344887hg38UCSC Ensembl
chr9:135219718..135220274hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38557
hg19557
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571942
Supporting Variants
Samples
Known GenesSETX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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