A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874429



Internal ID22649381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171214410..171220600hg38UCSC Ensembl
chr1:171183549..171189739hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg386191
hg196191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874429
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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