A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975585



Internal ID22750520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11369970..11369970hg38UCSC Ensembl
chr16:11463827..11463827hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372207
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975585
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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