A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18187089



Internal ID20754129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88271748..88272267hg38UCSC Ensembl
chr16:88305354..88305873hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6496830
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18187089
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0002


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