A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583366



Internal ID20956437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64125331..64126765hg38UCSC Ensembl
chr15:64417530..64418964hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381435
hg191435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18238801
Samples
Known GenesSNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583366
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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