A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038965



Internal ID21948308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42601335..42619597hg38UCSC Ensembl
chr15:42893533..42911795hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3818263
hg1918263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610864
Samples
Known GenesSTARD9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038965
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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