A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558979



Internal ID20932050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132347114..132347388hg38UCSC Ensembl
chr9:135222501..135222775hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7952n223
Supporting Variantsnssv18280092
Samples
Known GenesSETX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558979
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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