A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093894



Internal ID22003127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79438001..79438001hg38UCSC Ensembl
chr15:79730343..79730343hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600337
Samples
Known GenesKIAA1024
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093894
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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