A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17474729



Internal ID22532623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89305761..89320036hg38UCSC Ensembl
chr16:89372169..89386444hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3814276
hg1914276
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877424
Supporting Variants
Samples
Known GenesANKRD11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17474729
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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