A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547215



Internal ID16334624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104355226..104444794hg38UCSC Ensembl
Innerchr1:104897848..104987416hg19UCSC Ensembl
Innerchr1:104699371..104788939hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3889569
hg1989569
hg1889569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv447n54
Supporting Variantsnssv720210
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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