A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14314130



Internal ID22205140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:33402316..33402431hg38UCSC Ensembl
chr4:33403938..33404053hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198992
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14314130
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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