A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546174



Internal ID15986897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47416856..47417174hg38UCSC Ensembl
Innerchr1:47882528..47882846hg19UCSC Ensembl
Innerchr1:47655115..47655433hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38319
hg19319
hg18319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv260n54
Supporting Variantsnssv712911, nssv712912
Samples
Known GenesFOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546174
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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