A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271058



Internal ID20838098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105175714..105176740hg38UCSC Ensembl
chr6:105623589..105624615hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571365
Supporting Variants
Samples
Known GenesPOPDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271058
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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