A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280990



Internal ID20848031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:75141174..75141774hg38UCSC Ensembl
chr9:77756090..77756690hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557026
Supporting Variants
Samples
Known GenesOSTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280990
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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