A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280054



Internal ID20847094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130797148..130797637hg38UCSC Ensembl
chr9:133672535..133673024hg19UCSC Ensembl
Cytoband9q34.12
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557681
Supporting Variants
Samples
Known GenesABL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280054
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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