A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558528



Internal ID20931599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95154993..95155916hg38UCSC Ensembl
chr9:97917275..97918198hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18281521
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558528
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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