A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205768



Internal ID22354410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179178081..179178262hg38UCSC Ensembl
chr3:178895869..178896050hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14312021, nssv14312023, nssv14312022
SamplesNA19238, NA19239, NA19240
Known GenesPIK3CA
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3205768
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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