A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927814



Internal ID22703046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40334160..40334221hg38UCSC Ensembl
chr15:40626361..40626422hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388060
Samples
Known GenesC15orf52
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927814
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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