A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544869



Internal ID16332278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:54676..121042hg38UCSC Ensembl
Innerchr1:54676..121042hg19UCSC Ensembl
Innerchr1:44539..110905hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3866367
hg1966367
hg1866367
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1n54
Supporting Variantsnssv707619
Samples
Known GenesOR4F5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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