A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532171



Internal ID18483766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22007752..22508264hg38UCSC Ensembl
Innerchr14:22475991..22977249hg19UCSC Ensembl
Innerchr14:21545831..22047089hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38500513
hg19501259
hg18501259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036409
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)nssv3532171
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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