A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568646



Internal ID20941717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95890766..95891033hg38UCSC Ensembl
chr9:98653048..98653315hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281535
Samples
Known GenesERCC6L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568646
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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