A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610531



Internal ID16397940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15537635..15554099hg38UCSC Ensembl
Innerchr8:15395144..15411608hg19UCSC Ensembl
Innerchr8:15439515..15455979hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3816465
hg1916465
hg1816465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12013n54
Supporting Variantsnssv1156318
SamplesHGDP00274
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610531
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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