A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051911



Internal ID19141130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19802515hg38UCSC Ensembl
Innerchr14:19801743..20270674hg19UCSC Ensembl
Innerchr14:18871743..19340514hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38571567
hg19468932
hg18468772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1767n100
Supporting Variantsnssv3527277
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)nsv1051911
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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