A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17469900



Internal ID22527790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3066278..3080955hg38UCSC Ensembl
chr16:3116279..3130956hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3814678
hg1914678
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877463
Supporting Variants
Samples
Known GenesIL32
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17469900
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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