A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6575186



Internal ID20948257
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132902384..132906971hg38UCSC Ensembl
chr9:135777771..135782358hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg384588
hg194588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280109
Samples
Known GenesTSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6575186
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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