A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17409337



Internal ID22467207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4158049..4159259hg38UCSC Ensembl
chr20:4138696..4139906hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381211
hg191211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938921
Supporting Variants
Samples
Known GenesSMOX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17409337
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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