A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5968407



Internal ID22743342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65483873..65483873hg38UCSC Ensembl
chr16:65517776..65517776hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387285
Samples
Known GenesLINC00922
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5968407
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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