A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557366



Internal ID20930437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30722439..31099564hg38UCSC Ensembl
chr9:30722437..31099562hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38377126
hg19377126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280467
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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