A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1299n145



Internal ID22814315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:22726851..23979146hg38UCSC Ensembl
chrY:24872998..26125293hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg381252296
hg191252296
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111153, nsv3116105
Samplessample109, sample126, sample1, sample259
Known GenesBPY2, BPY2B, BPY2C, DAZ1, DAZ2, DAZ3, DAZ4, TTTY17A, TTTY17B, TTTY17C, TTTY3, TTTY3B, TTTY4, TTTY4B, TTTY4C
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1299n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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