A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559070



Internal ID20932141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4613035..4613665hg38UCSC Ensembl
chr9:4613035..4613665hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38631
hg19631
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280731
Samples
Known GenesSPATA6L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559070
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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