A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556564



Internal ID20929635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98000777..98001356hg38UCSC Ensembl
chr9:100763059..100763638hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281597
Samples
Known GenesANP32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556564
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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