A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589892



Internal ID16377301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21217943..21303734hg38UCSC Ensembl
Innerchr3:21259435..21345226hg19UCSC Ensembl
Innerchr3:21234439..21320230hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3885792
hg1985792
hg1885792
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8256n54
Supporting Variantsnssv1151756
SamplesNINDS_21
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589892
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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