A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092006



Internal ID22001239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74679594..74679594hg38UCSC Ensembl
chr15:74971935..74971935hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600963
Samples
Known GenesEDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092006
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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