A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116260



Internal ID21299526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:19454888..19476470hg38UCSC Ensembl
InnerchrY:21616774..21638356hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3821583
hg1921583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1295n145
Supporting Variantsnssv14102228
Samplessample189
Known GenesBCORP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116260
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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