A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468916



Internal ID21126469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95064501..95070700hg38UCSC Ensembl
chr11:94797665..94803863hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386200
hg196199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1279n223
Supporting Variantsnssv18196459
Samples
Known GenesSRSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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