A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036652



Internal ID19125871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18639702..19934411hg38UCSC Ensembl
Innerchr14:19416179..20402570hg19UCSC Ensembl
Innerchr14:18486179..19472410hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381294710
hg19986392
hg18986232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n100
Supporting Variantsnssv3713417
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, 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)nsv1036652
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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