A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562428



Internal ID20935499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127368466..127368785hg38UCSC Ensembl
chr9:130130745..130131064hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279951
Samples
Known GenesGARNL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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