A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6562596



Internal ID20935667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151786169..151786858hg38UCSC Ensembl
chr5:151165730..151166419hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38690
hg19690
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18268724
Samples
Known GenesG3BP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6562596
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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