A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547019



Internal ID16334428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103601221..103615727hg38UCSC Ensembl
Innerchr1:104143843..104158349hg19UCSC Ensembl
Innerchr1:103945366..103959872hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3814507
hg1914507
hg1814507
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv409n54
Supporting Variantsnssv719849
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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