A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530923



Internal ID18829204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19110155..19967215hg38UCSC Ensembl
Innerchr14:19697873..20435374hg19UCSC Ensembl
Innerchr14:18767873..19505214hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38857061
hg19737502
hg18737342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047860
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530923
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