A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567958



Internal ID20941029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102378851..103029215hg38UCSC Ensembl
chr9:105141133..105791497hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38650365
hg19650365
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279336
Samples
Known GenesCYLC2, LINC00587
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567958
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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