A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970855



Internal ID22745790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63378230..63378230hg38UCSC Ensembl
chr11:63145702..63145702hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358219
Samples
Known GenesMIR3680-1, MIR3680-2, SLC22A9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970855
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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