A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5979715



Internal ID22754650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:45316737..45316737hg38UCSC Ensembl
chr11:45338288..45338288hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38261
hg19261
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5979715
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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