A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589699



Internal ID16377108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:11996435..12042658hg38UCSC Ensembl
Innerchr3:12037909..12084158hg19UCSC Ensembl
Innerchr3:12012909..12059158hg18UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3846224
hg1946250
hg1846250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv959116
Samples
Known GenesSYN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589699
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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