A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv544874



Internal ID16332283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:364689..440332hg38UCSC Ensembl
Innerchr1:379005..454648hg19UCSC Ensembl
Innerchr1:368868..444511hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3875644
hg1975644
hg1875644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv707624
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv544874
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