A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040815



Internal ID19130034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19230949..19861566hg38UCSC Ensembl
Innerchr14:19801743..20329725hg19UCSC Ensembl
Innerchr14:18871743..19399565hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38630618
hg19527983
hg18527823
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1767n100
Supporting Variantsnssv3711126
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4M1, OR4N2, 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)nsv1040815
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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