A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224547



Internal ID20791587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60283606..60284886hg38UCSC Ensembl
chr11:60051079..60052359hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381281
hg191281
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584684
Supporting Variants
Samples
Known GenesMS4A4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00016


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