A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029429



Internal ID21938772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67242127..67242461hg38UCSC Ensembl
chr15:67534465..67534799hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610399
Samples
Known GenesAAGAB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029429
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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