A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3532606



Internal ID18830887
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 StatusS
Merged Variantsnsv1052876
Supporting Variants
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)nssv3532606
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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