A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036212



Internal ID19125431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19749402hg38UCSC Ensembl
Innerchr14:19801743..20217561hg19UCSC Ensembl
Innerchr14:18871743..19287401hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38518454
hg19415819
hg18415659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1767n100
Supporting Variantsnssv3527274
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)nsv1036212
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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