A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17377676



Internal ID22435546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67092697..67092697hg38UCSC Ensembl
chr16:67126600..67126600hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973859
Supporting Variants
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17377676
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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