A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556213



Internal ID20929284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35454914..35459109hg38UCSC Ensembl
chr9:35454911..35459106hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384196
hg194196
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280596
Samples
Known GenesATP8B5P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556213
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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