A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049532



Internal ID19138751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18605720..19873135hg38UCSC Ensembl
Innerchr14:19382197..20341294hg19UCSC Ensembl
Innerchr14:18452197..19411134hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381267416
hg19959098
hg18958938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n100
Supporting Variantsnssv3527005
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, 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)nsv1049532
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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