A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101878



Internal ID21289943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:18674215..18873549hg38UCSC Ensembl
InnerchrY:20836101..21035435hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38199335
hg19199335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110290
Supporting Variants
Samplessample53
Known GenesHSFY1, HSFY2, NCRNA00185, TTTY9A, TTTY9B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101878
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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