A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589968



Internal ID16377377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26381978..26396620hg38UCSC Ensembl
Innerchr3:26423469..26438111hg19UCSC Ensembl
Innerchr3:26398473..26413115hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3814643
hg1914643
hg1814643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8266n54
Supporting Variantsnssv960146, nssv960144, nssv960145
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589968
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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