A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830232



Internal ID22605167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49654372..49663952hg38UCSC Ensembl
chr1:50120044..50129624hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg389581
hg199581
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480472
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830232
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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