A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943511



Internal ID22718960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12318644..12335665hg38UCSC Ensembl
chr16:12412501..12429522hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3817022
hg1917022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv794n209
Supporting Variantsnssv17386582
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943511
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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