A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14338837



Internal ID22276470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33095433..33095535hg38UCSC Ensembl
chr10:33384361..33384463hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528490
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14338837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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