A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610530



Internal ID16397939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15531057..15554099hg38UCSC Ensembl
Innerchr8:15388566..15411608hg19UCSC Ensembl
Innerchr8:15432937..15455979hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3823043
hg1923043
hg1823043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12013n54
Supporting Variantsnssv1106863, nssv1106864
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610530
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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