A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590024



Internal ID16377433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28906200..29150601hg38UCSC Ensembl
Innerchr3:28947691..29192092hg19UCSC Ensembl
Innerchr3:28922695..29167096hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38244402
hg19244402
hg18244402
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8276n54
Supporting Variantsnssv960938, nssv960939
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590024
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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