A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5895622



Internal ID22670707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157244341..157302636hg38UCSC Ensembl
chr4:158165493..158223788hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3858296
hg1958296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420460
Samples
Known GenesGRIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5895622
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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