A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586392



Internal ID20959463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28715921..28736378hg38UCSC Ensembl
chr10:29004850..29025307hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3820458
hg1920458
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586392
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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