A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091906



Internal ID22001139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77198885..77198885hg38UCSC Ensembl
chr15:77491227..77491227hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602676
Samples
Known GenesPEAK1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091906
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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