A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549202



Internal ID16336611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:216459606..216477191hg38UCSC Ensembl
Innerchr1:216632948..216650533hg19UCSC Ensembl
Innerchr1:214699571..214717156hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3817586
hg1917586
hg1817586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv820n54
Supporting Variantsnssv736965
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549202
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