A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280059



Internal ID20847099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130827660..130828082hg38UCSC Ensembl
chr9:133703047..133703469hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571990
Supporting Variants
Samples
Known GenesABL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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