A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529692



Internal ID18827973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19032352..19957338hg38UCSC Ensembl
Innerchr14:19620039..20425497hg19UCSC Ensembl
Innerchr14:18690039..19495337hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38924987
hg19805459
hg18805299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043871
Supporting Variants
Samples
Known GenesBMS1P17, BMS1P18, OR11H2, OR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3529692
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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