A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589422



Internal ID16030145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4051238..4094550hg38UCSC Ensembl
Innerchr3:4092922..4136234hg19UCSC Ensembl
Innerchr3:4067922..4111234hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3843313
hg1943313
hg1843313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8178n54
Supporting Variantsnssv1152454, nssv958021
Samples1780854016_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589422
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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