A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830221



Internal ID22605156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47041287..47042386hg38UCSC Ensembl
chr1:47506959..47508058hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454531, nssv17468258
Samples
Known GenesCYP4X1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830221
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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