A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188177



Internal ID20755217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12015579..12016054hg38UCSC Ensembl
chr16:12109436..12109911hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38476
hg19476
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499095
Supporting Variants
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00034


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