A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14286938



Internal ID22324725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17722270..17722438hg38UCSC Ensembl
chr19:17833079..17833247hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3542757
Supporting Variants
SamplesNA19240
Known GenesMAP1S
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14286938
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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