A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039423



Internal ID19128642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98568588..98590299hg38UCSC Ensembl
Innerchr14:99034925..99056636hg19UCSC Ensembl
Innerchr14:98104678..98126389hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3821712
hg1921712
hg1821712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1967n100
Supporting Variantsnssv3532688, nssv3532702, nssv3532689, nssv3532686, nssv3532694, nssv3532697, nssv3532687, nssv3532690, nssv3532699, nssv3532701, nssv3532695, nssv3532692, nssv3532684, nssv3532698, nssv3532685, nssv3532693, nssv3532691, nssv3532700, nssv3532696
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)nsv1039423
Frequency
Sample Size11257
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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