A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901908



Internal ID22677061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6420263..6421780hg38UCSC Ensembl
chr4:6421990..6423507hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381518
hg191518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420994
Samples
Known GenesPPP2R2C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901908
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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