A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975860



Internal ID22750795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66887946..66887946hg38UCSC Ensembl
chr16:66921849..66921849hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375028
Samples
Known GenesPDP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975860
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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