A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588274



Internal ID20961345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78480458..78481667hg38UCSC Ensembl
chr15:78772800..78774009hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381210
hg191210
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239727
Samples
Known GenesIREB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588274
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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