A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995839



Internal ID21905182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174704015..174705819hg38UCSC Ensembl
chr4:175625166..175626970hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381805
hg191805
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545115
Samples
Known GenesGLRA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995839
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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