A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280871



Internal ID20847911
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 StatusS
Merged Variantsnsv6563970
Supporting Variants
Samples
Known GenesABHD17B, C9orf57, C9orf85, GDA, TMEM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280871
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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