A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6087777



Internal ID21997010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74681461..74681461hg38UCSC Ensembl
chr15:74973802..74973802hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606652
Samples
Known GenesEDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6087777
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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