A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592127



Internal ID20965198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72299040..72299534hg38UCSC Ensembl
chr15:72591381..72591875hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241873
Samples
Known GenesCELF6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592127
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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