A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563970



Internal ID20937041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71164626..72130108hg38UCSC Ensembl
chr9:73779542..74745024hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38965483
hg19965483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18280871
Samples
Known GenesABHD17B, C9orf57, C9orf85, GDA, TMEM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563970
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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