A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036303



Internal ID19125522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18661498..19954424hg38UCSC Ensembl
Innerchr14:19437975..20422583hg19UCSC Ensembl
Innerchr14:18507975..19492423hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381292927
hg19984609
hg18984449
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n100
Supporting Variantsnssv3528018, nssv3528023, nssv3714196, nssv3528016, nssv3528027, nssv3528017, nssv3528021, nssv3528025, nssv3528020, nssv3528022, nssv3528026, nssv3528019, nssv3528028, nssv3714197, nssv3528024
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K1, OR4K2, OR4K5, 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)nsv1036303
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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