A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6561547



Internal ID20934618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92150559..92151953hg38UCSC Ensembl
chr8:93162787..93164181hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7422n223
Supporting Variantsnssv18279039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6561547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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