A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14312144



Internal ID22168127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10667741..10667842hg38UCSC Ensembl
chr4:10669365..10669466hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526030
Supporting Variants
SamplesHG00514
Known GenesCLNK
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14312144
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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