A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386591



Internal ID22444461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11855946..11855946hg38UCSC Ensembl
chr16:11949803..11949803hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386591
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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