A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590475



Internal ID16377884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65190441..65229010hg38UCSC Ensembl
Innerchr3:65176116..65214685hg19UCSC Ensembl
Innerchr3:65151156..65189725hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3838570
hg1938570
hg1838570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8353n54
Supporting Variantsnssv1151911
SamplesHGDP01310
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590475
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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