A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527291



Internal ID18825572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19749402hg38UCSC Ensembl
Innerchr14:19802529..20217561hg19UCSC Ensembl
Innerchr14:18872529..19287401hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38518454
hg19415033
hg18414873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042440
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nssv3527291
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