A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052627



Internal ID19141846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62471651..62485899hg38UCSC Ensembl
Innerchr14:62938369..62952617hg19UCSC Ensembl
Innerchr14:62008122..62022370hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3814249
hg1914249
hg1814249
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531054
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052627
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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