A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540692



Internal ID20913981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21248904..21249505hg38UCSC Ensembl
chr1:21575397..21575998hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18248513
Samples
Known GenesECE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540692
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