A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590025



Internal ID16377434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:28906200..29159969hg38UCSC Ensembl
Innerchr3:28947691..29201460hg19UCSC Ensembl
Innerchr3:28922695..29176464hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg38253770
hg19253770
hg18253770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8276n54
Supporting Variantsnssv960940
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590025
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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