A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934650



Internal ID22709980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12468503..12468660hg38UCSC Ensembl
chr16:12562360..12562517hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379248
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934650
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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