A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316985



Internal ID22260005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156660547..156660684hg38UCSC Ensembl
chr4:157581699..157581836hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526137
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316985
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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