A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116879



Internal ID21300145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:11042694..11550798hg38UCSC Ensembl
InnerchrY:13198370..13706474hg19UCSC Ensembl
CytobandYq11.1
Allele length
AssemblyAllele length
hg38508105
hg19508105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101873
Samplessample43
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116879
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