A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114052



Internal ID21297318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:19453650..19477615hg38UCSC Ensembl
InnerchrY:21615536..21639501hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3823966
hg1923966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1295n145
Supporting Variantsnssv14102224, nssv14102303
Samplessample184, sample407
Known GenesBCORP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114052
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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