A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560717



Internal ID20933788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14329521..14330188hg38UCSC Ensembl
chr9:14329520..14330187hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38668
hg19668
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280182
Samples
Known GenesNFIB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560717
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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