A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280732



Internal ID20847772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4616097..4616683hg38UCSC Ensembl
chr9:4616097..4616683hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566243
Supporting Variants
Samples
Known GenesSPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280732
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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