A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15761399



Internal ID22095890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93504000..93504000hg38UCSC Ensembl
chr15:94047229..94047229hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4447147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsSVTYPE=INS;REPTYPE=DUP
ReferenceGenome_in_a_Bottle
Pubmed ID32541955
Accession Number(s)nssv15761399
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer