A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17362233



Internal ID22587902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20119207..20121236hg38UCSC Ensembl
chr10:20408136..20410165hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg382030
hg192030
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5915806
Supporting Variants
Samples
Known GenesPLXDC2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17362233
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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