A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041442



Internal ID19130661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19869145..19934411hg38UCSC Ensembl
Innerchr14:20337304..20402570hg19UCSC Ensembl
Innerchr14:19407144..19472410hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3865267
hg1965267
hg1865267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1790n100
Supporting Variantsnssv3530701
Samples
Known GenesOR4K2, OR4K5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041442
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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