A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838433



Internal ID22613368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:171913882..171927683hg38UCSC Ensembl
chr4:172835033..172848834hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3813802
hg1913802
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500332
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838433
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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