A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586357



Internal ID20959428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116661290..116662910hg38UCSC Ensembl
chr10:118420801..118422421hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg381621
hg191621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv895n223
Supporting Variantsnssv18224581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586357
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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