A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051236



Internal ID19140455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38483785..38569955hg38UCSC Ensembl
Innerchr14:38952989..39039159hg19UCSC Ensembl
Innerchr14:38022740..38108910hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3886171
hg1986171
hg1886171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1873n100
Supporting Variantsnssv3712285, nssv3712286
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)nsv1051236
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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