A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587609



Internal ID20960680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76402428..76403098hg38UCSC Ensembl
chr11:76113472..76114142hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230364
Samples
Known GenesLOC100506127
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587609
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