A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6585371



Internal ID20958442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17386384..17387443hg38UCSC Ensembl
chr10:17428383..17429442hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg381060
hg191060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224537
Samples
Known GenesST8SIA6, ST8SIA6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6585371
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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