A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581801



Internal ID20954872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33096598..33097109hg38UCSC Ensembl
chr15:33388799..33389310hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38512
hg19512
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239508
Samples
Known GenesFMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581801
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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