A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052166



Internal ID19141385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22155699..22491833hg38UCSC Ensembl
Innerchr14:22623632..22960820hg19UCSC Ensembl
Innerchr14:21693472..22030660hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38336135
hg19337189
hg18337189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1805n100
Supporting Variantsnssv3532206
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)nsv1052166
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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