A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928173



Internal ID22703408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14491267..14493729hg38UCSC Ensembl
chr16:14585124..14587586hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg382463
hg192463
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17371993
Samples
Known GenesPARN
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928173
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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