A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050861



Internal ID19140080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22173768..22481502hg38UCSC Ensembl
Innerchr14:22641665..22950491hg19UCSC Ensembl
Innerchr14:21711505..22020331hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38307735
hg19308827
hg18308827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1805n100
Supporting Variantsnssv3532238
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)nsv1050861
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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