A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567611



Internal ID20940682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77499574..77500307hg38UCSC Ensembl
chr9:80114490..80115223hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7838n223
Supporting Variantsnssv18281072
Samples
Known GenesGNA14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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