A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590477



Internal ID16377886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65192321..65226921hg38UCSC Ensembl
Innerchr3:65177996..65212596hg19UCSC Ensembl
Innerchr3:65153036..65187636hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3834601
hg1934601
hg1834601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8353n54
Supporting Variantsnssv963680, nssv1151912, nssv963679
SamplesNINDS_83
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590477
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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