A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532238



Internal ID18830519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22173768..22481502hg38UCSC Ensembl
Innerchr14:22641665..22950491hg19UCSC Ensembl
Innerchr14:21711505..22020331hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38307735
hg19308827
hg18308827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050861
Supporting Variants
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)nssv3532238
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