A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv547021



Internal ID16334430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103601627..103614388hg38UCSC Ensembl
Innerchr1:104144249..104157010hg19UCSC Ensembl
Innerchr1:103945772..103958533hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3812762
hg1912762
hg1812762
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv409n54
Supporting Variantsnssv719852, nssv719851
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv547021
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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