A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968215



Internal ID22743151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4900456..4900456hg38UCSC Ensembl
chr16:4950457..4950457hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371489
Samples
Known GenesPPL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968215
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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