A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530660



Internal ID18828941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19742826..19934411hg38UCSC Ensembl
Innerchr14:20210985..20402570hg19UCSC Ensembl
Innerchr14:19280825..19472410hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38191586
hg19191586
hg18191586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041479
Supporting Variants
Samples
Known GenesOR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530660
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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