A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931284



Internal ID22706566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64692128..64692245hg38UCSC Ensembl
chr15:64984327..64984444hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388368
Samples
Known GenesOAZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931284
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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