A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592351



Internal ID20965422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80613343..80614478hg38UCSC Ensembl
chr15:80905684..80906819hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381136
hg191136
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2604n223
Supporting Variantsnssv18239769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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