A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565809



Internal ID20938880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13926045..13935151hg38UCSC Ensembl
chr9:13926044..13935150hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg389107
hg199107
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280174
Samples
Known GenesLINC00583
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565809
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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