A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv610869



Internal ID16051592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:29058875..29114041hg38UCSC Ensembl
Innerchr8:28916392..28971558hg19UCSC Ensembl
Innerchr8:28972311..29027477hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3855167
hg1955167
hg1855167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1109358
Samples
Known GenesKIF13B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv610869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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