A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611459



Internal ID16398868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:67083031..67102984hg38UCSC Ensembl
Innerchr8:67995266..68015219hg19UCSC Ensembl
Innerchr8:68157820..68177773hg18UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3819954
hg1919954
hg1819954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1115737
Samples
Known GenesCSPP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611459
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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