A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111153



Internal ID21294419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22726851..23839694hg38UCSC Ensembl
InnerchrY:24872998..25985841hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg381112844
hg191112844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1299n145
Supporting Variantsnssv14102209, nssv14102255, nssv14102204
Samplessample109, sample126, sample259
Known GenesBPY2, BPY2B, BPY2C, DAZ1, DAZ2, DAZ3, DAZ4, TTTY17A, TTTY17B, TTTY17C, TTTY4, TTTY4B, TTTY4C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111153
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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