A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045206



Internal ID18787737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18302217..19852919hg38UCSC Ensembl
Innerchr14:19078694..20321078hg19UCSC Ensembl
Innerchr14:18148694..19390918hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381550703
hg191242385
hg181242225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1753n100
Supporting Variantsnssv3526898
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, OR11H2, OR4M1, OR4N2, 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)nsv1045206
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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