A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565922



Internal ID20938993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121504982..121505159hg38UCSC Ensembl
chr9:124267261..124267438hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565922
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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