A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225494



Internal ID20792534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125864775..125865542hg38UCSC Ensembl
chr10:127553344..127554111hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38768
hg19768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588466
Supporting Variants
Samples
Known GenesDHX32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225494
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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