A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591322



Internal ID20964393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78599788..78600394hg38UCSC Ensembl
chr15:78892130..78892736hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239731
Samples
Known GenesCHRNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591322
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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