A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883465



Internal ID22658445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13558706..13560894hg38UCSC Ensembl
chr1:13885201..13887389hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382189
hg192189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883465
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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