A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580077



Internal ID20953148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74967566..74968753hg38UCSC Ensembl
chr11:74678611..74679798hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381188
hg191188
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230868
Samples
Known GenesSPCS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580077
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