A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610265



Internal ID16397674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10383901..10433056hg38UCSC Ensembl
Innerchr8:10241411..10290566hg19UCSC Ensembl
Innerchr8:10278821..10327976hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3849156
hg1949156
hg1849156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11952n54
Supporting Variantsnssv1106250
Samples
Known GenesMSRA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610265
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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