A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279642



Internal ID20846682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113394012..113394425hg38UCSC Ensembl
chr9:116156292..116156705hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562917
Supporting Variants
Samples
Known GenesALAD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279642
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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