A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236013



Internal ID20803053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13292736..13293555hg38UCSC Ensembl
chr10:13334736..13335555hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591879
Supporting Variants
Samples
Known GenesPHYH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236013
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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