A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6560289



Internal ID20933360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143537932..143539537hg38UCSC Ensembl
chr4:144459085..144460690hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg381606
hg191606
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264759
Samples
Known GenesSMARCA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6560289
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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