A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562733



Internal ID22431479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127777012..127777012hg38UCSC Ensembl
chr3:127495855..127495855hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307981, nssv14307980
SamplesNA19239, NA19240
Known GenesMGLL
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562733
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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