A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564178



Internal ID16351587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:30917220..30948610hg38UCSC Ensembl
Innerchr14:31386426..31417816hg19UCSC Ensembl
Innerchr14:30456177..30487567hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3831391
hg1931391
hg1831391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3606n54
Supporting Variantsnssv1148941
SamplesHGDP01249
Known GenesSTRN3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564178
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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