A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052876



Internal ID19142095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:94186416..94277392hg38UCSC Ensembl
Innerchr14:94652753..94743729hg19UCSC Ensembl
Innerchr14:93722506..93813482hg18UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg3890977
hg1990977
hg1890977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1958n100
Supporting Variantsnssv3532606
Samples
Known GenesPPP4R4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052876
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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