A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580949



Internal ID20954020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116537247..116538443hg38UCSC Ensembl
chr10:118296759..118297955hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226665
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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