A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102233



Internal ID21273606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:12297713..12510602hg38UCSC Ensembl
InnerchrY:14418438..14622404hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38212890
hg19203967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111965
Supporting Variants
Samplessample193
Known GenesGYG2P1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102233
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer