A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590054



Internal ID16377463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:35442172..35496239hg38UCSC Ensembl
Innerchr3:35483664..35537731hg19UCSC Ensembl
Innerchr3:35458668..35512735hg18UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3854068
hg1954068
hg1854068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962131
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590054
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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