A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102260



Internal ID21279070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:9802750..9919557hg38UCSC Ensembl
InnerchrY:9640359..9757166hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38116808
hg19116808
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114542
Supporting Variants
Samplessample277
Known GenesTTTY22, TTTY23, TTTY23B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102260
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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