A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17480059



Internal ID22537962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:49259163..49276756hg38UCSC Ensembl
chr1:49724835..49742428hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3817594
hg1917594
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5830228
Supporting Variants
Samples
Known GenesAGBL4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17480059
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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