A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547322



Internal ID16334731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105862418..105954525hg38UCSC Ensembl
Innerchr1:106405040..106497147hg19UCSC Ensembl
Innerchr1:106206563..106298670hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3892108
hg1992108
hg1892108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv720711
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547322
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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