A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589853



Internal ID16030576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:18344240..18386958hg38UCSC Ensembl
Innerchr3:18385732..18428450hg19UCSC Ensembl
Innerchr3:18360736..18403454hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3842719
hg1942719
hg1842719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151743
SamplesNINDS_91
Known GenesSATB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589853
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