A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935780



Internal ID22711125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42612000..42615039hg38UCSC Ensembl
chr15:42904198..42907237hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg383040
hg193040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385055
Samples
Known GenesSTARD9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935780
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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