A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050899



Internal ID19140118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22173768..22496192hg38UCSC Ensembl
Innerchr14:22641665..22965177hg19UCSC Ensembl
Innerchr14:21711505..22035017hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38322425
hg19323513
hg18323513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1805n100
Supporting Variantsnssv3532239
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050899
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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