A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14368644



Internal ID22259887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109694117..109694117hg38UCSC Ensembl
chr13:110346464..110346464hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560010
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14368644
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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