A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196667



Internal ID22346642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23939282..23939482hg38UCSC Ensembl
chr14:24408491..24408691hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2556n152
Supporting Variantsnssv14444950
SamplesHG00733
Known GenesDHRS4-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196667
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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