A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279369



Internal ID20846409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104706730..105087346hg38UCSC Ensembl
chr9:107469011..107849627hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38380617
hg19380617
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562158
Supporting Variants
Samples
Known GenesABCA1, LOC286367, NIPSNAP3A, NIPSNAP3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279369
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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