A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388515



Internal ID22268683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62687392..62688188hg38UCSC Ensembl
chr16:62721296..62722092hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3213544
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388515
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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