A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6094304



Internal ID22003537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80974152..80974152hg38UCSC Ensembl
chr15:81266493..81266493hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6094304
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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