A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17383914



Internal ID22441784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84647295..84647295hg38UCSC Ensembl
chr16:84680901..84680901hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17383914
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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