A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102248



Internal ID21276363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:3295912..3507916hg38UCSC Ensembl
InnerchrY:3163953..3375957hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38212005
hg19212005
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3115477
Supporting Variants
Samplessample235
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102248
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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