A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16923807



Internal ID16632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213717318..213720980hg38UCSC Ensembl
chr2:214582042..214585704hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg383663
hg193663
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446012
Supporting Variants
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16923807
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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