A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384153



Internal ID22442023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11209005..11209005hg38UCSC Ensembl
chr16:11302862..11302862hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5977649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384153
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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