A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549461



Internal ID16336870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:241391303..241476101hg38UCSC Ensembl
Innerchr1:241554603..241639401hg19UCSC Ensembl
Innerchr1:239621226..239706024hg18UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3884799
hg1984799
hg1884799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv739143
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549461
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer