A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591025



Internal ID16378434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:95747651..95772892hg38UCSC Ensembl
Innerchr3:95466495..95491736hg19UCSC Ensembl
Innerchr3:96949185..96974426hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3825242
hg1925242
hg1825242
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv968079
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591025
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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