A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944585



Internal ID21364654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69300568..69300699hg38UCSC Ensembl
chr15:69592907..69593038hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15184094
SamplesHG002
Known GenesPAQR5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944585
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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