A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117942



Internal ID21301208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrY:12287023..12292262hg38UCSC Ensembl
InnerchrY:14407725..14412965hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg385240
hg195241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14102300
Samplessample394
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117942
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