A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528200



Internal ID18826481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18976182..19831523hg38UCSC Ensembl
Innerchr14:19562127..20299682hg19UCSC Ensembl
Innerchr14:18632127..19369522hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38855342
hg19737556
hg18737396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046960
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, 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)nssv3528200
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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