A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532244



Internal ID18830525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22185576..22486728hg38UCSC Ensembl
Innerchr14:22653472..22955716hg19UCSC Ensembl
Innerchr14:21723312..22025556hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38301153
hg19302245
hg18302245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047956
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)nssv3532244
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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