A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6569695



Internal ID20942766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132347150..132347380hg38UCSC Ensembl
chr9:135222537..135222767hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7952n223
Supporting Variantsnssv18280093
Samples
Known GenesSETX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6569695
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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