A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567587



Internal ID20940658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36205750..36206902hg38UCSC Ensembl
chr9:36205747..36206899hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280612
Samples
Known GenesCLTA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567587
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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