A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17405331



Internal ID22463201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59721842..59740559hg38UCSC Ensembl
chr20:58296897..58315614hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3818718
hg1918718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5963564
Supporting Variants
Samples
Known GenesPHACTR3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17405331
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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