A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900116



Internal ID22675255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:91087684..91298543hg38UCSC Ensembl
chr4:92008835..92219694hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38210860
hg19210860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424519
Samples
Known GenesCCSER1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900116
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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