A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838901



Internal ID22613836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:22446910..22448424hg38UCSC Ensembl
chr4:22448533..22450047hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381515
hg191515
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494364
Samples
Known GenesGPR125
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838901
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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