A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584684



Internal ID20957755
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 StatusM
Merged Variants
Supporting Variantsnssv18224547
Samples
Known GenesMS4A4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584684
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