A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589959



Internal ID16377368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25988740..26123044hg38UCSC Ensembl
Innerchr3:26030231..26164535hg19UCSC Ensembl
Innerchr3:26005235..26139539hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38134305
hg19134305
hg18134305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8265n54
Supporting Variantsnssv960130
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589959
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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