A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546177



Internal ID16333586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47416856..47417336hg38UCSC Ensembl
Innerchr1:47882528..47883008hg19UCSC Ensembl
Innerchr1:47655115..47655595hg18UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38481
hg19481
hg18481
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv263n54
Supporting Variantsnssv712921, nssv712916, nssv712918, nssv712920, nssv712917, nssv712919, nssv712915
Samples
Known GenesFOXE3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546177
Frequency
Sample Size17421
Observed Gain5
Observed Loss2
Observed Complex0
Frequencyn/a


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