A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564441



Internal ID20937512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73802792..73803882hg38UCSC Ensembl
chr8:74715027..74716117hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381091
hg191091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278680
Samples
Known GenesUBE2W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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