A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594441



Internal ID20967512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33129860..33131287hg38UCSC Ensembl
chr15:33422061..33423488hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18239509
Samples
Known GenesFMN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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