A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101879



Internal ID21290794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:21366872..21490464hg38UCSC Ensembl
InnerchrY:23528758..23652350hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg38123593
hg19123593
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114151
Supporting Variants
Samplessample64
Known GenesCYorf17, RBMY2EP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101879
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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