A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558495



Internal ID20931566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74991227..74992216hg38UCSC Ensembl
chr9:77606143..77607132hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38990
hg19990
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280982
Samples
Known GenesC9orf41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558495
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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