A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541934



Internal ID20915202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:214286627..214287063hg38UCSC Ensembl
chr1:214459970..214460406hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248560
Samples
Known GenesSMYD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541934
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer