A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590483



Internal ID16377892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65199224..65230129hg38UCSC Ensembl
Innerchr3:65184899..65215804hg19UCSC Ensembl
Innerchr3:65159939..65190844hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3830906
hg1930906
hg1830906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8353n54
Supporting Variantsnssv1151919, nssv963706, nssv963711, nssv963709, nssv1151918, nssv963710, nssv1151921, nssv1151920, nssv963708, nssv963707, nssv963705
SamplesNINDS_70, 1798860280_A, 1780854197_A, 1780854362_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590483
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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