A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042373



Internal ID19131592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19924615..19956767hg38UCSC Ensembl
Innerchr14:20392774..20424926hg19UCSC Ensembl
Innerchr14:19462614..19494766hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3832153
hg1932153
hg1832153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1795n100
Supporting Variantsnssv3530720
Samples
Known GenesOR4K1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042373
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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