A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288055



Internal ID20497273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36188763..36188763hg38UCSC Ensembl
chr18:33768726..33768726hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751294
Supporting Variants
Samples
Known GenesMOCOS
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288055
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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