A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561614



Internal ID20934685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111921039..111921605hg38UCSC Ensembl
chr9:114683319..114683885hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279570
Samples
Known GenesUGCG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561614
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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