A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590117



Internal ID16377526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41053800..41097611hg38UCSC Ensembl
Innerchr3:41095291..41139102hg19UCSC Ensembl
Innerchr3:41070295..41114106hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3843812
hg1943812
hg1843812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8288n54
Supporting Variantsnssv962395
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590117
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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