A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559996



Internal ID20933067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54007035..54008039hg38UCSC Ensembl
chr8:54919595..54920599hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278230
Samples
Known GenesTCEA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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