A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564579



Internal ID20937650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77568391..77569809hg38UCSC Ensembl
chr9:80183307..80184725hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg381419
hg191419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281075
Samples
Known GenesGNA14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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