A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592487



Internal ID20965558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:28657393..28658492hg38UCSC Ensembl
chr10:28946322..28947421hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592487
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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