A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052037



Internal ID19141256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19881689..19955201hg38UCSC Ensembl
Innerchr14:20349848..20423360hg19UCSC Ensembl
Innerchr14:19419688..19493200hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3873513
hg1973513
hg1873513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1790n100
Supporting Variantsnssv3530706
Samples
Known GenesOR4K1, OR4K5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052037
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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