A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589833



Internal ID20962904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78486431..78486552hg38UCSC Ensembl
chr15:78778773..78778894hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239728
Samples
Known GenesIREB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589833
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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