A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217544



Internal ID20784584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:16590187..16590964hg38UCSC Ensembl
chr10:16632186..16632963hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38778
hg19778
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577329
Supporting Variants
Samples
Known GenesRSU1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217544
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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