A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17384257



Internal ID22442127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77339122..77339893hg38UCSC Ensembl
chr16:77373019..77373790hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38772
hg19772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928514
Supporting Variants
Samples
Known GenesADAMTS18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17384257
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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