A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611809



Internal ID16052532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:98913400..99081282hg38UCSC Ensembl
Innerchr8:99925628..100093510hg19UCSC Ensembl
Innerchr8:99994804..100162686hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38167883
hg19167883
hg18167883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118156
Samples
Known GenesOSR2, STK3, VPS13B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611809
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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