A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584278



Internal ID20957349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68915528..68918126hg38UCSC Ensembl
chr10:70675284..70677882hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382599
hg192599
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230386
Samples
Known GenesDDX50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584278
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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