A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589888



Internal ID16377297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21215817..21303734hg38UCSC Ensembl
Innerchr3:21257309..21345226hg19UCSC Ensembl
Innerchr3:21232313..21320230hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3887918
hg1987918
hg1887918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8256n54
Supporting Variantsnssv1151751, nssv1151752
SamplesHGDP00695, NINDS_96
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589888
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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