A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115229



Internal ID21298495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:9227571..9229687hg38UCSC Ensembl
InnerchrY:9065180..9067296hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg382117
hg192117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102290, nssv14102275
Samplessample368, sample321
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115229
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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