A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589397



Internal ID16376806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3538765..3594980hg38UCSC Ensembl
Innerchr3:3580449..3636664hg19UCSC Ensembl
Innerchr3:3555449..3611664hg18UCSC Ensembl
Cytoband3p26.2
Allele length
AssemblyAllele length
hg3856216
hg1956216
hg1856216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152444
SamplesHGDP00815
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589397
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