A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054356



Internal ID18796887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22064075..22501578hg38UCSC Ensembl
Innerchr14:22532339..22970562hg19UCSC Ensembl
Innerchr14:21602179..22040402hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38437504
hg19438224
hg18438224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1803n100
Supporting Variantsnssv3532173
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)nsv1054356
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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