A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527068



Internal ID18825349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18639702..19791792hg38UCSC Ensembl
Innerchr14:19416179..20259951hg19UCSC Ensembl
Innerchr14:18486179..19329791hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381152091
hg19843773
hg18843613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054743
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4M1, OR4Q3, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527068
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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