A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464477



Internal ID21122030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:90732696..90743429hg38UCSC Ensembl
chr11:90465864..90476597hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3810734
hg1910734
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182213
Samples
Known GenesDISC1FP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464477
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