A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102292



Internal ID21285099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:22208726..22376449hg38UCSC Ensembl
InnerchrY:24354873..24522596hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38167724
hg19167724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111566
Supporting Variants
Samplessample369
Known GenesLOC100652931, RBMY1F, RBMY2FP, TTTY5
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102292
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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