A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5888448



Internal ID22663454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:161498448..161498656hg38UCSC Ensembl
chr4:162419600..162419808hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428499
Samples
Known GenesFSTL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5888448
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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