A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908189



Internal ID22683399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6708495..6710331hg38UCSC Ensembl
chr11:6729726..6731562hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908189
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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