A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479059



Internal ID22536961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68570372..68600779hg38UCSC Ensembl
chr16:68604275..68634682hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3830408
hg1930408
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5876237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479059
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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