A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv548838



Internal ID16336247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:196844140..196911099hg38UCSC Ensembl
Innerchr1:196813270..196880229hg19UCSC Ensembl
Innerchr1:195079893..195146852hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3866960
hg1966960
hg1866960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv753n54
Supporting Variantsnssv734057
Samples
Known GenesCFHR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv548838
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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