A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15184094



Internal ID21322890
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944585
Supporting Variants
SamplesHG002
Known GenesPAQR5
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15184094
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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