A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051708



Internal ID19140927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19908195..19954424hg38UCSC Ensembl
Innerchr14:20376354..20422583hg19UCSC Ensembl
Innerchr14:19446194..19492423hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3846230
hg1946230
hg1846230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1794n100
Supporting Variantsnssv3712126
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)nsv1051708
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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