A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038500



Internal ID19127719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22167785..22490838hg38UCSC Ensembl
Innerchr14:22635681..22959826hg19UCSC Ensembl
Innerchr14:21705521..22029666hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38323054
hg19324146
hg18324146
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1806n100
Supporting Variantsnssv3532234
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)nsv1038500
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