A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970055



Internal ID22744990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118732023..118732023hg38UCSC Ensembl
chr11:118602732..118602732hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360788
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970055
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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