A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545377



Internal ID15986100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9537178..9542904hg38UCSC Ensembl
Innerchr1:9597237..9602962hg19UCSC Ensembl
Innerchr1:9519824..9525549hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg385727
hg195726
hg185726
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709712
Samples
Known GenesSLC25A33
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545377
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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