A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5947419



Internal ID22722924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74214192..74219909hg38UCSC Ensembl
chr15:74506533..74512250hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg385718
hg195718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5947419
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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