A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14383670



Internal ID22181553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100526599..100526706hg38UCSC Ensembl
chr14:100992936..100993043hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV duplication
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223685
Supporting Variants
SamplesHG00514
Known GenesWDR25
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14383670
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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