A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527297



Internal ID18825578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19784261hg38UCSC Ensembl
Innerchr14:19802529..20252420hg19UCSC Ensembl
Innerchr14:18872529..19322260hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38553313
hg19449892
hg18449732
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054350
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4M1, 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)nssv3527297
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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