A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590460



Internal ID16377869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65036271..65091801hg38UCSC Ensembl
Innerchr3:65021946..65077476hg19UCSC Ensembl
Innerchr3:64996986..65052516hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3855531
hg1955531
hg1855531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151910
Samples1780854599_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590460
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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