A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280939



Internal ID20847979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72908148..72909389hg38UCSC Ensembl
chr9:75523064..75524305hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381242
hg191242
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574546
Supporting Variants
Samples
Known GenesALDH1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280939
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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