A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584123



Internal ID20957194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78467648..78467903hg38UCSC Ensembl
chr15:78759990..78760245hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239726
Samples
Known GenesIREB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584123
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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