A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562302



Internal ID20935373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35765398..35766105hg38UCSC Ensembl
chr9:35765395..35766102hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38708
hg19708
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562302
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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