A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3526836



Internal ID18478431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19169707hg38UCSC Ensembl
Innerchr14:19002112..19801743hg19UCSC Ensembl
Innerchr14:18072112..18871743hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38944073
hg19799632
hg18799632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035372
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3526836
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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