A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17477711



Internal ID22535612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26482718..26487522hg38UCSC Ensembl
chr16:26494039..26498843hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384805
hg194805
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5874189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17477711
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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