A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101870



Internal ID21280611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:19453106..19477437hg38UCSC Ensembl
InnerchrY:21614992..21639323hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3824332
hg1924332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110828
Supporting Variants
Samplessample30
Known GenesBCORP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101870
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