A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941909



Internal ID22717340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70403514..70403652hg38UCSC Ensembl
chr15:70695853..70695991hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38139
hg19139
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384253
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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