A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17479098



Internal ID22537000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72059037..72061873hg38UCSC Ensembl
chr16:72092936..72095772hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg382837
hg192837
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878270
Supporting Variants
Samples
Known GenesHP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17479098
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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