A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547534



Internal ID16334943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110916672..110942585hg38UCSC Ensembl
Innerchr1:111459294..111485207hg19UCSC Ensembl
Innerchr1:111260817..111286730hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3825914
hg1925914
hg1825914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173115
SamplesHGDP00003
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547534
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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