A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6027595



Internal ID21936938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76382073..76384855hg38UCSC Ensembl
chr15:76674414..76677196hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382783
hg192783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598681
Samples
Known GenesSCAPER
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6027595
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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