A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594280



Internal ID20967351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94551358..94551882hg38UCSC Ensembl
chr10:96311115..96311639hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222325
Samples
Known GenesHELLS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594280
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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