A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592957



Internal ID20966028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103252849..103253029hg38UCSC Ensembl
chr10:105012606..105012786hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225987
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592957
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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