A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562451



Internal ID20935522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:158685053..158762870hg38UCSC Ensembl
chr5:158112061..158189878hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3877818
hg1977818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267407
Samples
Known GenesEBF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562451
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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