A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099484



Internal ID22008717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40784481..40784481hg38UCSC Ensembl
chr15:41076679..41076679hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg382921
hg192921
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608614
Samples
Known GenesDNAJC17
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099484
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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