A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226850



Internal ID20793890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51382007..51382877hg38UCSC Ensembl
chr13:51956143..51957013hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38871
hg19871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584843
Supporting Variants
Samples
Known GenesINTS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226850
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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