A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564687



Internal ID20937758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:134306212..134306401hg38UCSC Ensembl
chr5:133641903..133642092hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18267299
Samples
Known GenesCDKL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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